IQVIA

Job OverviewWe are seeking a reliable and detail-oriented accounting professional to join our team, supporting Accounts Payable and financial operations in line with IQVIA Finance Standard Operating Procedures, US GAAP, and SOX requirements. In this role, you will play a key part in ensuring accurate and timely processing of financial transactions while maintaining strong relationships with internal stakeholders and external vendors. This position offers an excellent opportunity for an experienced AP professional who thrives in a structured yet dynamic, compliance-driven environment. Key ResponsibilitiesProcess and validate third-party invoices in Coupa and SAP, ensuring accuracy and compliance with company policies.Execute daily Accounts Payable operations, maintaining high standards of efficiency and precision.Support month-end closing activities, ensuring timely and accurate reporting.Act as a point of contact for internal stakeholders and vendors, resolving inquiries in a professional and timely manner.Prepare and deliver reports to management to support decision-making and financial oversight.Ensure compliance with internal financial procedures, SOX controls, and relevant accounting standards (US GAAP/local GAAP).Contribute to continuous process improvements within AP and financial operations.Perform additional accounting and finance-related duties as assigned.Qualifications & ExperienceBachelor’s degree in Accounting, Finance, or a related field (or higher).Minimum of 4 years of experience in Accounting, Accounts Payable, or Procurement.Strong working knowledge of ERP systems such as SAP; experience with Coupa, ServiceNow, or other procurement systems is an advantage.Proficiency in Microsoft Office applications, particularly Excel.Strong data analysis and data handling skills with high attention to detail.Ability to apply judgment within established procedures to resolve issues effectively.Excellent organizational skills with the ability to prioritize multiple tasks and meet deadlines.Strong interpersonal and communication skills, with the ability to build and maintain effective working relationships across teams and stakeholders.What We OfferA stable and professional environment within a global organization.Opportunities to deepen your expertise in accounting and compliance frameworks.Collaboration with international teams and exposure to global financial processes.A role where accuracy, ownership, and continuous improvement are highly valued.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Responsible for the on-time completion of primary market research consulting projects or components of large, complex projects for clients in the life sciences field. Essential Functions Project Delivery & Execution Participates or leads team in the design, development and delivery of primary market research consulting projects or components of larger, complex projects. Reviews and analyzes client requirements or problems and assists in the development of proposals and research materials that ensure high client satisfaction. Provides direction and guidance to project team members including field team, programming and statistical services where relevant assigned to engagement. Pevelops detailed documentation and specifications. Performs qualitative and/or quantitative analyses to assist in the identification of client issues and the development of client-specific deliverables. Designs, structures and delivers client reports and presentations that are appropriate to the characteristics or needs of the audience. Supports project manager to effectively deliver findings to clients in form of in-person or virtual sessions. Recommends improvements and alternative solutions to resolve problems. Provides follow-up with client after project deliverable has been completed to ensure client satisfaction. When acting as Project Manager, proactively manages project timelines and manages day-to-day communication with the client and team members. Ability to bring innovation and adopt AI-driven solutions. Knowledge Development Proactively develops broader and deeper knowledge of related primary market research methodologies and life science consulting through on-the-job experience and participation in training opportunities. Participate in developing subject matter expertise in life sciences and healthcare. Qualifications Bachelor’s Degree required. 2–4 years of related experience in primary market research consulting and/or life sciences industry required. Possesses solid project management skills and client influencing and relationship-building skills. Works willingly and effectively with others in and across the organization to accomplish team goals. Experienced with developing consultative relationships with stakeholders at clients in the life science industry. Ability to manage multiple projects, juggle priorities and deliver on tight deadlines. Knowledge of primary research and analytical methodologies, tools and techniques related to functional area. Knowledge of key issues and current developments in the life science industry. Excellent presentation and communication skills. Has necessary subject matter expertise to effectively manage projects within a given center of excellence. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Conseiller(ère) principal(e) et statisticien(ne), recherche centrée sur le patient Présentation Chez IQVIA, l’équipe Solutions centrées sur le patient aide les clients à générer des données probantes solides sur l’expérience des patients dans l’ensemble du développement clinique, des soumissions réglementaires et de la diffusion scientifique. Notre équipe Statistiques et psychométrie est spécialisée dans l’analyse des données d’évaluations des résultats cliniques (COA) et des résultats rapportés par les patients (PRO), en combinant rigueur scientifique et conseil stratégique afin de soutenir des décisions à fort impact dans le développement de médicaments. Le rôle En tant que conseiller(ère) principal(e), vous dirigerez ou soutiendrez les analyses statistiques pour des projets impliquant des données COA/PRO. Vous contribuerez à la planification des analyses, à leur exécution, à leur interprétation et à la production de rapports à leur sujet, ainsi qu’à la communication avec les clients, afin de fournir des données probantes scientifiquement solides, pertinentes sur le plan réglementaire et clairement communiquées. Principales responsabilités Diriger le volet d’analyse quantitative pour des projets de complexité modérée, en assurant une exécution de haute qualité, dans les délais et scientifiquement rigoureuse. Élaborer et réviser les plans d’analyse, les maquettes de sorties, les spécifications des livrables, les exigences de programmation, les résultats statistiques et les rapports techniques. Appliquer des méthodes statistiques avancées aux données COA/PRO. Interpréter les résultats de manière claire et crédible pour les équipes internes et les clients, et communiquer les choix méthodologiques de façon à soutenir la prise de décision. Contribuer à la génération de données probantes pertinentes pour les autorités réglementaires et les payeurs, notamment en appui à la stratégie des indicateurs de résultats et à la communication scientifique. Établir de solides relations de travail avec les clients et les équipes internes interfonctionnelles, et contribuer aux propositions, aux soutenances d’offres et aux activités de développement des affaires. Contribuer à la gestion du périmètre du volet d’analyse quantitative, y compris les objectifs, les échéances et la qualité des livrables. Encadrer les membres moins expérimentés de l’équipe et contribuer au développement des compétences de l’équipe, à la formation, aux normes et à l’amélioration des processus. Qualifications Maîtrise ou doctorat en biostatistique, en statistique, en psychométrie, en recherche sur les résultats, en épidémiologie ou dans un domaine quantitatif connexe. Plus de 5 ans d’expérience pertinente dans l’industrie pharmaceutique, biotechnologique, des ORC, des soins de santé ou dans le conseil. Connaissance approfondie des méthodes statistiques complexes applicables aux essais cliniques de phases I à IV (analyse multivariée, analyse de régression, analyse logistique, analyse de survie, modèles mixtes à mesures répétées, etc.). Connaissance de SAS et/ou R. Excellentes compétences en communication écrite et orale, grande attention aux détails et capacité à travailler efficacement dans un environnement collaboratif matriciel. Pourquoi nous rejoindre Ce rôle offre l’occasion de travailler sur des recherches spécialisées, centrées sur le patient, qui éclairent le développement clinique, la stratégie réglementaire et la communication des données probantes dans un large éventail de domaines thérapeutiques. Vous rejoindrez une équipe mondiale collaborative dotée d’une expertise approfondie en analyse des COA, en psychométrie et en méthodologie statistique avancée. Senior Consultant and Statistician, Patient-Centered Research Location: Remote, candidates must be based in Canada Overview At IQVIA, the Patient Centered Solutions team helps clients generate robust evidence on the patient experience across clinical development, regulatory submissions, and scientific dissemination. Our Statistics & Psychometrics team specializes in the analysis of clinical outcome assessment (COA) and patient-reported outcomes (PRO) data, combining scientific rigor with strategic consulting to support high-impact decisions in drug development. The Role As a Senior Consultant, you will lead or support statistical analyses for projects involving COA/PRO data. You will contribute across analysis planning, execution, interpretation, reporting, and client communication, helping deliver evidence that is scientifically sound, regulatory-relevant, and clearly communicated. Key Responsibilities Lead the quantitative analysis workstream for projects of moderate complexity, ensuring high-quality, timely, and scientifically sound delivery. Develop and review analysis plans, output shells, output specifications, programming requirements, statistical outputs, and technical reports. Apply advanced statistical methods to COA/PRO data. Interpret results clearly and credibly for internal teams and clients and communicate methodological choices in a way that supports decision-making. Contribute to regulatory- and payer-relevant evidence generation, including support for endpoint strategy and scientific communication. Build strong working relationships with clients and cross-functional internal teams, and contribute to proposals, bid defenses, and business development activities. Assists in managing the scope of the quantitative analysis workstream, including objectives, timelines and quality of deliverables. Mentor junior team members and contribute to team capability building, training, standards, and process improvement. Qualifications Master’s degree or PhD in biostatistics, statistics, psychometrics, outcomes research, epidemiology, or a related quantitative field. 5+ years of relevant experience in the pharmaceutical, biotech, CRO, healthcare, or consulting environment. Advanced knowledge of complex statistical methods that apply to Phase I-IV clinical trials (multivariate analysis, regression analysis, logistic analysis, survival analysis, mixed models repeated measures, etc.) Familiarity with SAS and/or R. Excellent written and verbal communication skills, strong attention to detail, and the ability to work effectively in a collaborative, matrixed environment. Why Join Us This role offers the opportunity to work on specialized, patient-centered research that informs clinical development, regulatory strategy, and evidence communication across a wide range of therapeutic areas. You will join a collaborative global team with deep expertise in COA analysis, psychometrics, and advanced statistical methodology. IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $114,100.00 - $164,100.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $114,100.00 - $164,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.

Are you passionate about improving patient access to innovative therapies? Join our team as a Business Access Manager in Northern Italy, where you'll play a key role in expanding access to cutting-edge biosimilar medicines in Piemonte, Valle d’Aosta and Lombardia. This is an exciting opportunity to work with a leading biopharmaceutical company that is dedicated to bringing high-quality biologics to market at cost-effective prices. Job Overview:  In this role, you will manage commercial activities and engage with hospital stakeholders to promote a range of specialist biosimilar products. You will collaborate with colleagues to provide decision-makers with the necessary information for optimal adoption and prescribing. Your responsibilities include establishing our client as a trusted partner in the biosimilars/biologics market, collecting and reporting relevant data, and achieving sales and market share growth. Qualifications: Pharmaceutical sales experience within hospitals, especially with high-cost drug pharmacists within hospitals. Experience in biosimilars or therapy areas such as Rare Disease, Haematology, Nephrology, Ophthalmology, Immunology, Oncology, Endocrinology, Orthopaedics, or Rheumatology. Life Sciences degree or equivalent; advanced degrees in Business Administration or Health Economics are a plus. Strong relationship-building skills with both external and internal customers. Fluent in Italian and English. Willingness to travel regularly throughout the territory. Full driving license essential. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Clinical Research Coordinator in Middlesborough Working Hours: 24 hours per week Start Date: ImmediatelyDuration: Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Middlesborough. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. Key Responsibilities As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including: Prescreening and Screening tasksReview charts from the site data baseMaintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systemsSupporting patient screening and enrollment, including handling informed consent and privacy documentationCoordinating logistical activities for study procedures in line with the study protocolProcessing lab samplesPerforming data entry, quality checks, and resolving queries to ensure data accuracy and completenessPatient educationCommunicating with study monitors and responding to study-related inquiriesCarrying out general administrative tasks related to the studyYour ProfileWe are looking for candidates who bring a combination of education, experience, and skills: Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedulesGood knowledge of medical terminologyStrong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial siteExcellent interpersonal and communication skillsStrong organizational skills and attention to detailFluency in EnglishWhy Join IQVIA?At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference. Interested?If this sounds like the right opportunity for you, we encourage you to apply today. Please note we cannot offer sponsorship for these positions. #LI-HCPN #LI-CES #LI-DNP #LI-CT1 #LI-Onsite IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview: The Medical Information Case Processor responsibilities include receiving and documenting incoming telephone calls or emails from investigative sites or other sources reporting Lifecycle Safety Data.Responsibilities include: Medical Information Case processor responsibilities include receiving and documenting incoming calls, chats, and emails from external customers such as patients and/or healthcare providers) and responding to their enquiries about products. Summarizing these reports based on information identified as vital to the projectDisseminate clear, accurate information to healthcare professionals and patients based on the approved call scripts and/or other approved resources related to the use of client productsCreating Adverse Event and Product Quality Complaint reports requiring concise data entry covering everything from patient symptoms, admission and results – this will include medical terminology, writing narratives, generating case queries.Clarify, investigate and capture adverse event and product quality information Essential Functions Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming - Adverse Events(AE)/endpoint informationEnsure to meet quality standards per project requirements.To demonstrate problem solving capabilities. Qualifications Bachelor's degree in life sciences or related field.Languages: Advanced English level (French desirable)1-3 years of experience in pharmacovigilance activities (desirable)Good knowledge of medical terminology.Excellent attention to detail and accuracy.Strong organizational skills and time management skills.Strong verbal/written communication skills.Self-motivated and flexible.Work modality: 100% home-based IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Medical Assistant / Phlebotomist to support patient care by delivering in-home diagnostic services. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.    Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.     Qualifications:  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  If located in the state of Washington or Louisiana, a state issued CMA or CPT license is required.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Essential Functions•    Resource Headcount management including existing, attrition and new hire. Analysis versus Budget and Forecast on a monthly basis•    Track joiners moving into / out of teams and ensure profiles creation in enterprise tools of the organization•    Maintain and upkeep of data related to resources (Rate card, Utilization targets, team/product related information)•    Planning and executing periodic Skills assessment process – reporting progress and reporting / analytics of Skills data•    Update and maintain resource project assignments and schedules on enterprise tools•    Tracking resource bandwidth/availability using excel and enterprise tools. Work with Resource managers and Line managers through regular cadence on data validity and accuracy•    Standard/ad-hoc reports and dashboards related to headcount, utilization, compliance and Availability•    Contractors’ extension tracking•    Follow up and tracking of non-billable hours’ analysis and reporting to management Experience & Qualifications•    Graduate in Sciences, Commerce or Engineering subjects•    3-6 years of Business Operations/PMO/Resource management experience in a MNC company, with exposure to Technology, Analytics, Data Management skills, projects and methodologies. Experience in a Life Sciences/Pharma company is an advantage•    Experience in using HR/Finance/Resource Management enterprise applications is a must. Salesforce knowledge, specifically CRM and PSA, is a definite plus •    Excellent written and verbal communication in English is mandatory•    Advanced Excel skills is mandatory. Should have proficiency in Outlook, PowerPoint, Word and other Microsoft Office applications•    Should have experience in using SharePoint, OneNote and TEAMS•    Problem solving and logical reasoning skills are a must IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA HCPN has an exciting position in Spain for an exciting freelance CRA. Basic Functions:Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.Responsibilities Participates in the investigator recruitment process, performing site evaluation visits of potential investigators to evaluate the capability of the site to successfully manage and conduct the clinical study.Coordinate activities with the site and internal departments in preparation for the initiation of the study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF and EDC system; monitoring activities and study close-out activities.Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs.Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data.May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.Assists with, and attends, Investigator Meetings for assigned studies.Attends study-related, company, departmental, and external meetings, as required.Ensures all study deliverables are completed per IQVIA Biotech and study timelinesConducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs.Serves as mentor for junior CRAs and those new to the company and/or study.KNOWLEDGE, SKILLS AND ABILITIES: Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.Experience in monitoring and/or coordinating clinical trials required.Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals.Able to handle several priorities within multiple, complex trials.Able to reason independently and recommend specific solutions in clinical settings.Able to work independently, prioritize, and work within a matrix team environment.Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.If this role sounds of interest, please apply today! #LI-DNP #LI-CES #LI-HCPN #LI-CT1 IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Are you looking for an opportunity as a Clinical Research Nurse?  Do you want to work for an industry leading company. This part-time role is to support a clinical trial in Madrid. We are looking for candidates with the following skills and experience: BS/BA in life sciences or educational equivalent in a clinical environment as a nurseBasic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedulesStrong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and WordExcellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client​Good organizational skills with the ability to pay close attention to detail.#LI-DNP #LI-HCPN #LI-CES #LI-CT1 IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Purpose: Manage a series of localisation projects cost–effectively, efficiently and to the highest quality standards in our industry. This will involve the effective coordination of in-house and external suppliers as well as technological resources. In addition, the Project Manager will provide support to Team Lead/Senior Project Managers and Head of Operations as and when required. Project Management and administration including: Preparing quotes and timelines based on client requirements and seeking approval by Team Lead/Senior Project Manager/Head of Operations where relevant.  Supporting the Team Lead/Senior Project Manager/Head of Operations with the development of new training and processes. Selecting appropriate resources from a database of translation professionals, ensuring that we can supply when required the correct breadth of languages, experience, cost and expertise. Coordination of human and technical resources to achieve the successful completion of projects and jobs. Liaising with customers. Monitoring deadlines and budgets. Achieving agreed deadlines. Effective use of MemoQ and Portico. Providing excellent customer service. Participating actively in client calls and meetings. Completing other tasks as requested by Team Lead/Senior Project Managers or Head of Operations.  Accountabilities and Responsibilities Quality of Output. Adherence to agreed work practices. Supplier selection and control. Operating within project budgets, monitoring profitability. Project completion. Maintaining a clear, well organised structure for projects. Delegating tasks to team members as appropriate. Providing support for junior colleagues. Building and maintaining client relationships. Taking responsibility for accurately planning all necessary stages of a project lifecycle. Taking responsibility for seeking support as and when required and ensuring daily and weekly planner is up-to-date. ​Experience and Skills Excellent communication skills - both written and verbal, with strong numeric and analytical skills. Highly motivated, with demonstrated problem solving and organisational skills.  Flexible and adaptable enough to be able to work in a variety of roles in a rapidly changing environment. Ability to work calmly and effectively under pressure in order to prioritise workload and meet client deadlines. Knowledge of a foreign language an advantage. Ability to take responsibility and ownership and use initiative. Excellent attention to detail. Enthusiasm and inclination to learn. Willingness to share expertise. 1-2 years Project Management experience. Team player. Graduate - ideally with a language/translation degree. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. We are seeking a highly skilled and experienced market research professional to supervise the monitoring and maintenance of the ChannelDynamics Global Panel. As a key member of the ChannelDynamics Global team, the CD Offering Manager will manage and monitor all aspects of the global syndicated panel operations as well as ad-hoc panel projects. The ideal candidate will have a strong background in panel design and monitoring, with a focus on delivering high-quality results. ChannelDynamics has seen significant growth over the past 7 years and this role will be key in driving ongoing development and growth. Essential Functions: Lead and manage international syndicated panel projects within the pharmaceuticals sector. Design and implement research panels to gather data for the ChannelDynamics database. Monitor and analyze panel data to ensure accuracy and reliability. Collaborate with cross-functional teams to scope and determine budgets and timelines Develop and maintain relationships with key stakeholders and external partners. Ensure compliance with industry regulations and best practices in market research. Prepare and present detailed reports and presentations to senior management.  Be key point of contact for all CD panel operations monitoring, maintenance and development, related to existing deliverables, new client demand and sales operations support in executing on panel design and launch Seek efficiencies and innovative ways to improve CD syndicated panel participation across 36 countries with a focus on priority markets and specialty panels Support technical & commercial teams through clear communication of requirements around both methodology and participation reporting Consult, develop, and implement pilot projects, ad-hoc projects and new syndicated panels Ensure continuous monitoring of all panel activity with supporting documentation, reporting mechanisms and associated analytics and collateral Work with internal COEs and external agencies to plan, coordinate, implement and monitor project execution Our Ideal Candidate Will Have: Bachelor's degree in Market Research, Business, Pharmaceuticals, or a related field. 5 years’ experience working in international pharmaceuticals / life science market research and HCP panel design, ideally in a syndicated offering PLEASE SUBMIT YOUR CV IN ENGLISH. APPLICANTS SHOULD HAVE THE RIGHT TO WORK IN THE COUNTRY THEY ARE APPLYING TO! We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

QVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. We are seeking an Associate Sales Operations Manager to support the optimization and execution of sales processes, performance reporting, and business operations. This role partners closely with Sales, Finance, and cross-functional teams to drive operational excellence, improve data-driven decision-making, and support business growth. Key Responsibilities Manage sales reporting, dashboards, and performance metrics.Analyze sales data to identify trends, opportunities, and areas for improvement.Support forecasting, pipeline management, and business reviews.Drive process improvements to enhance sales productivity and operational efficiency.Ensure data accuracy and integrity across CRM and reporting tools.Collaborate with stakeholders to implement sales programs and operational initiatives.Qualifications Bachelor’s degree in Business, Finance, Analytics, or related field.3+ years of experience in Sales Operations, Business Operations, Analytics, or a related function.Strong analytical and problem-solving skills.Experience with CRM platforms (e.g., Salesforce) and reporting tools.Advanced Excel skills; Power BI experience is a plus.Strong communication and stakeholder management abilities.Ability to manage multiple priorities in a fast-paced environment.Preferred Skills Experience supporting sales organizations in a technology or services environment.Knowledge of sales forecasting, KPI tracking, and process optimization.Continuous improvement mindset with a focus on operational excellence.Join us and help drive scalable, data-driven sales operations that enable business success. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Aperçu du poste Grâce à une expertise inégalée en immunologie, IQVIA Laboratories se positionne comme l’un des principaux fournisseurs de services spécialisés dans le développement et l’analyse de tests biologiques dans les domaines de l’infectiologie, du métabolisme et de l’oncologie. Notre équipe multidisciplinaire de scientifiques, appuyée par des plateformes technologiques de pointe, a joué un rôle déterminant dans le développement, la qualification et la validation de tests utilisés dans plus de 100 dossiers soumis à la FDA pour l’approbation de nouvelles entités moléculaires, incluant des vaccins majeurs, des antiviraux, des immunothérapies ainsi que des produits de thérapie génique ou de thérapie cellulaire. IQVIA souhaite recruter un(e) Partenaire d’Affaires Senior – Ressources Humaines (Hybride) dans le cadre d’un contrat à durée déterminée d’environ 12 mois. Le ou la Partenaire d’Affaires RH Senior est responsable de la gestion efficace des ressources humaines à travers l’organisation. Ce rôle comprend la mise en œuvre, le maintien et l’amélioration continue des politiques, procédures et pratiques RH, tout en assurant la conformité avec les lois et réglementations du travail applicables au Québec. Ce poste soutient principalement notre laboratoire situé à Laval (environ 250 employés), tout en collaborant également avec des partenaires et clients à l’international. Responsabilités principales Partenariat RH et collaboration Établir de solides partenariats avec les équipes RH spécialisées et les Centres d’excellence (ex. : HRPSC, Finance PSC) afin d’assurer une prestation harmonieuse des programmes RH.Offrir du coaching, du soutien et des conseils aux membres plus juniors de l’équipe RH.Conformité, politiques et gouvernance RH Effectuer des revues de conformité, incluant l’analyse de la législation du travail, les exercices en matière d’équité salariale, ainsi que les audits des systèmes, processus et documents RH.Proposer des recommandations et accompagner les gestionnaires dans la compréhension et l’application des exigences RH.Développer, mettre à jour et implanter les politiques et procédures RH selon les besoins organisationnels et la réglementation québécoise.Santé et sécurité & soutien au laboratoire BSL3 Collaborer étroitement avec l’équipe de Santé et sécurité pour assurer la conformité aux lois, normes et protocoles internes.Gérer les dossiers CNESST en collaboration avec la Coordonnatrice RH.Assurer un rôle clé dans le soutien RH au laboratoire BSL3 (CL3), notamment concernant les habilitations de sécurité, la surveillance médicale, les protocoles post-exposition, la conformité et le soutien opérationnel continu.Programmes RH et initiatives globales Diriger ou soutenir la mise en œuvre des programmes RH locaux et globaux, tels que :Cycle annuel de rémunérationCycle d’évaluation de performanceProgrammes de développement du leadershipPlanification des talents et de la relèvePartenariat stratégique auprès des unités d’affaires Fournir un accompagnement RH quotidien, du coaching aux gestionnaires et un soutien stratégique aux unités d’affaires assignées (site de Laval et unité globale basée aux États-Unis).Utiliser les données, indicateurs de performance (KPIs) et analyses pour éclairer les décisions et soutenir les discussions avec les leaders.Changements organisationnels et transformation Participer aux initiatives de transformation organisationnelle, incluant :RéorganisationsInitiatives de restructuration et de réduction des coûts (au besoin)Changements liés à la conception organisationnelleGarantir que toutes les activités respectent la législation québécoise et sont appuyées par une gestion efficace du changement.Rapports et gestion des cas Préparer des rapports RH, tableaux de bord et analyses pour soutenir la prise de décision de la haute direction.Répondre aux demandes et enjeux RH, en gérant les dossiers de façon autonome ou en collaboration avec les leaders RH.Qualifications Baccalauréat requis.Minimum de 4 ans d’expérience en ressources humaines, dans un rôle généraliste ou mixte généraliste/spécialiste, ou expérience équivalente.Excellente connaissance des lois du travail applicables au Québec.Grandes habiletés en coaching et accompagnement.Capacité démontrée en leadership.Excellentes aptitudes en résolution de problèmes, jugement et prise de décision.Habiletés en présentation et en influence.Maîtrise de la suite Microsoft Office et des systèmes RH.Excellentes habiletés de communication orale et écrite, avec de fortes aptitudes interpersonnelles.Très grand sens de la confidentialité et de la discrétion.Forte attention aux détails.Capacité à travailler efficacement dans un environnement matriciel.Habileté démontrée à mener des projets.Capacité à établir et maintenir de solides relations de travail avec collègues, gestionnaires et clients.En raison des interactions fréquentes avec des clients locaux et internationaux, la maîtrise du français et de l’anglais est requise.** Veuillez noter qu’il s’agit d’un poste hybride et que la personne sélectionnée devra être en mesure de se déplacer au bureau au moins 2 à 3 jours par semaine. _____________________________________________ Job OverviewWith unparalleled expertise in immunology IQVIA Laboratories is one of the leading service providers in the development and analysis of specialized biological assays in the fields of infectiology, metabolism, and oncology. Our multidisciplinary team of scientists, equipped with state-of-the-art technological platforms, has played a critical role in the development, qualification, and validation of assays, as well as their high‑throughput application, in more than 100 submissions associated with FDA approval of new molecular entities, including major vaccines, antivirals, and immunotherapy, gene therapy, or cell therapy products. IQVIA is seeking an outstanding candidate to join our team as a Senior Human Resources Business Partner (Hybrid) on a fixed‑term contract of approximately 12 months. The Senior HR Business Partner is responsible for ensuring effective HR management across the organization. This includes leading the implementation, maintenance, and continuous improvement of HR policies, procedures, and practices, while ensuring full compliance with employment laws and regulations in Québec. This role primarily supports our Laval-based laboratory in Canada (approx. 250 employees), while also collaborating with global clients. Essential Functions HR Partnership & Collaboration Build strong partnerships with HR specialist teams and Centers of Excellence (e.g., HRPSC, Finance PSC) to ensure alignment and seamless delivery of HR programs.Provide coaching, guidance, and support to junior HR team members as needed.Compliance, Policies & HR Governance Conduct HR compliance and policy reviews, including employment legislation assessments, salary equity exercises, and audits of HR systems, processes, and documentation.Recommend updates and support managers in understanding and applying HR requirements.Develop, implement, and update HR policies and procedures based on organizational needs and Québec legislation.Health & Safety and BSL3 Support Partner closely with the Health & Safety team to ensure compliance with relevant laws, regulations, and internal protocols.Manage CNESST cases collaboratively with the HR Coordinator.Play a key HR role supporting our BSL3 (CL3) laboratory, including managing security clearance, medical surveillance, post‑exposure protocols, compliance, and ongoing operational HR support.HR Programs & Global Initiatives Lead or support the implementation of local and global HR programs such as:Annual compensation cyclePerformance cycleLeadership development programsTalent and succession planningHR Business Partnering Provide day‑to‑day HR partnering, management coaching, and strategic support to assigned business units (Laval site and a U.S.-based global business unit).Use data, KPIs, and analytics to drive decision‑making and support leadership discussions.Organizational Change & Transformation Participate in organizational change and transformation initiatives, including:ReorganizationsRestructuring and cost‑saving initiatives (if applicable)Organizational design changesEnsure all transformation activities are compliant with local legislation and supported through effective change management approaches.Reporting & Case Management Prepare HR reports, dashboards, and data analyses to support senior leadership decisions.Respond to and resolve HR queries, managing cases independently or in collaboration with senior HR leaders.Qualifications Bachelor’s Degree required.Minimum 4 years of experience in an HR generalist role or a combination of generalist/specialist experience, or an equivalent combination of education, training, and experience.Extensive knowledge of Québec and relevant employment legislation.Strong coaching and counseling skills.Effective leadership ability.Excellent problem-solving, judgment, and decision‑making skills.Strong presentation and influencing abilities.Proficiency in Microsoft Office and HRIS systems.Strong verbal and written communication skills with excellent interpersonal abilities.High level of discretion and confidentiality.Strong attention to detail.Ability to work effectively within a matrix environment.Proven project leadership capability.Ability to build and maintain effective working relationships with colleagues, managers, and clients.Due to frequent interactions with local and global clients, bilingualism in French and English is required.**  Please note that this is a hybrid position, and the selected candidate must be able to commute to the office at least 2–3 days per week. IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $79,700.00 - $132,800.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $79,700.00 - $132,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für unseren Kunden, ein renommiertes, international agierendes Familienunternehmen, suchen wir zum nächstmöglichen Zeitpunkt einen Pharmaberater (m/w/d) General Medicine / Diabetes Im Gebiet: Konstanz, Albstadt, Tuttlingen Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Verordnung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast idealerweise bereits erste Erfahrung im Pharma-Außendienst gesammelt, idealerweise in der Indikation Diabetes. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, Dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für Dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du kannst mit digitalen Medien gut umgehen und hast solide Kenntnisse, um auch englische Fachtexte zu verstehen. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater; #Biologie; #Chemie; #Pharmareferent; #BTA; #CTA; #PTA; #Oecotrophologie; #Pharmazie; #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Coordonnateur(trice) des services de projets en laboratoireIQVIA Laboratories — Poste en télétravail au Canada **Le ou la candidat(e) doit résider au Canada pour être admissible à ce poste. Nous recrutons des innovateurs passionnés qui font progresser le secteur de la santé grâce à une collaboration réfléchie et inclusive. Si vous souhaitez découvrir une carrière porteuse de sens, joignez‑vous à nous pour transformer et accélérer la recherche et le développement. Le ou la Coordonnateur(trice) des services de projets en laboratoire soutient les projets de laboratoire clinique tout au long du cycle d’étude en coordonnant les opérations quotidiennes, en assurant le suivi de la performance des études et en garantissant des livrables de haute qualité pour nos clients. Ce que vous ferezCoordonner les activités de démarrage d’étude : comptes rendus, suivis d’actions et documents de laboratoire spécifiques au protocole. Soutenir la surveillance centralisée de laboratoire et contribuer à la mise en place des exigences propres au protocole. Gérer les tâches opérationnelles quotidiennes telles que le chargement des sites, l’accès au Portail des investigateurs et l’expédition des trousses. Assurer le suivi de la performance des études à l’aide d’outils de monitoring pour identifier les tendances et escalader les enjeux. Répondre aux questions et demandes liées au protocole en collaboration avec les équipes internes et les parties prenantes externes. Assurer la communication avec les clients lorsque le gestionnaire de projet est absent. Participer aux audits et inspections et soutenir la formation des sites, des ARC et des clients. Coordonner la clôture des projets en respectant les normes organisationnelles et les exigences du protocole. Ce que nous recherchonsDiplôme d’études secondaires ou équivalent; un baccalauréat en sciences de la vie ou domaine connexe est un atout. Minimum d’un an d’expérience pertinente dans les secteurs clinique, médical ou de la santé. Maîtrise des outils informatiques (Word, Excel, PowerPoint). Toute combinaison équivalente de formation, d’études et d’expérience peut être acceptée en remplacement du diplôme Les connaissances, compétences et habiletés requisesExcellentes aptitudes en communication, relations interpersonnelles et gestion des parties prenantes. Solides compétences organisationnelles et de gestion du temps dans un environnement dynamique. Capacité d’analyse, de résolution de problèmes et de prise de décision. Connaissance des outils de suivi d’étude, de la documentation et de la coordination interfonctionnelle. Vous devrez travailler directement avec des départements, des équipes, des fonctions de support et des parties prenantes d'IQVIA situés partout au Canada et à travers le monde, par conséquent, une connaissance fonctionnelle de l'anglais, tant à l'écrit qu'à l'oral, est nécessaire à l'exercice des fonctions de ce poste. Ce que nous vous offronsNous plaçons nos employés au cœur de tout ce que nous faisons et nous nous engageons à leur offrir, ainsi qu’à leurs familles, des avantages qui répondent à leurs besoins diversifiés et en constante évolution. Nous investissons dans des programmes intégrés de mieux‑être pour soutenir leur santé physique, mentale, émotionnelle, financière et sociale, afin qu’ils puissent s’épanouir à la maison comme au travail, à chaque étape de leur parcours. Pour en savoir plus sur nos avantages, visitez https://jobs.iqvia.com/benefits. Si vous souhaitez libérer votre potentiel, joignez‑vous à IQVIA Laboratories pour contribuer à rendre l’extraordinaire possible. ------------------------------------------------------------------------------------------------ Laboratory Project Services Coordinator IQVIA Laboratories — Remote position in Canada *Candidate must reside in Canada to be eligible for this position. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Lab Project Services Coordinator supports clinical laboratory projects throughout the full study lifecycle by coordinating daily operations, monitoring study performance, and ensuring high‑quality, timely deliverables for customers. What You’ll Be DoingCoordinate study start‑up activities including meeting minutes, action logs, and protocol‑specific laboratory documentation. Support centralized laboratory monitoring and assist with protocol‑specific setup requirements. Manage daily operational tasks such as site loading, Investigator Portal access, and kit shipment coordination. Monitor study performance using dashboards and tools to identify trends and escalate issues proactively. Respond to study queries by collaborating with internal teams and external stakeholders. Lead customer communication during periods when the Project Manager is unavailable. Participate in audits and inspections and support training for sites, CRAs, and customers. Coordinate project close‑out ensuring compliance with protocol and organizational standards. What We Are Looking ForHigh School Diploma or equivalent; Bachelor’s degree in Life Sciences or related field preferred. Minimum 1 year of relevant experience in clinical, medical, or healthcare environments. Technical proficiency with standard computer applications (Word, Excel, PowerPoint). Other Equivalent combination of education, training, and experience may be accepted in lieu of degree. The Knowledge, Skills and Abilities Needed for This RoleStrong communication, interpersonal, and stakeholder‑management skills. Excellent organizational and time‑management abilities in a fast‑paced environment. Critical thinking and problem‑solving skills to address study issues effectively. Proficiency with study documentation, monitoring tools, and cross‑functional coordination. What We Offer YouWe put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial and social well‑being so they can thrive at home and at work, at any stage of their well‑being journey. To learn more about our benefits, visit https://jobs.iqvia.com/benefits. If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible! You will be required to work directly with IQVIA departments, teams, support functions and stakeholders located across Canada and around the world therefore, a functional knowledge of English, both written and spoken, is necessary to perform the duties of this position. IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $53,300.00 - $88,900.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $53,300.00 - $88,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.

We are seeking an Associate Principal Scientist to join IQVIA Laboratories in Indiana.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.Job Summary:The Associate Principal Scientist provides scientific leadership in in vitro and in vivo metabolism and biotransformation studies, with a primary focus on mass spectrometry data interpretation, metabolite profiling, and rapid, high‑quality reporting to support drug discovery and development programs.What You’ll Be Doing:Independently analyze, interpret, and report MS and MS/MS data from in vitro and in vivo metabolism studiesDevelop, implement, and troubleshoot analytical methods for metabolite identification and profilingAssign metabolite structures and propose metabolic pathways using sound scientific judgmentManage study flow to ensure high‑quality, on‑time delivery of reports in a fast‑paced, high‑throughput environmentServe as a scientific resource for complex data interpretation, assay development, and problem solvingCollaborate with project teams and interact with clients to discuss scientific principles and study outcomesMentor and provide guidance to junior scientists and new team membersWhat We Are Looking For:PhD, Master’s, or Bachelor’s degree in chemistry, biochemistry, biology, or a related scientific discipline.In‑depth experience with drug metabolism and biotransformation, including metabolite profiling and structural elucidationStrong expertise in mass spectrometry, including MS and MS/MS data collection and interpretationHands‑on knowledge of analytical method development and troubleshooting for metabolism studiesOther Equivalent combination of education, training, and experience may be accepted in lieu of degreeThe Knowledge, Skills and Abilities Needed for This Role:Ability to rapidly interpret complex data and produce clear, concise scientific reports under tight timelinesStrong understanding of ADME metabolism principles and high‑throughput discovery workflowsExcellent written and verbal communication skills with the ability to engage internal teams and clientsDemonstrated attention to detail, sound scientific judgment, and commitment to data qualityAbility to manage multiple projects simultaneously in a production‑driven CRO environmentWhat We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial and social well‑being so they can thrive at home and at work, at any stage of their well‑being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $80,200.00 - $167,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Purpose Under guidance, maintain and enhance complex reference data files to support IQVIA production processes, with a focus on drug information classification, product coding, and data accuracy. Essential Functions • Perform research (e.g., internet search, databases, publications, and external sources) to gather and verify drug information to improve completeness and accuracy of IQVIA reference data • Classify pharmaceutical products using standard classification systems such as ATC, NFC, CHC, and others • Process, validate, and analyze data using SQL, Excel, or Python • Ensure accuracy and integrity of data by validating information sourced from third parties before updating records • Support production processes by generating required data files and outputs for quality control and client deliverables • Perform a variety of tasks including data input, report validation, and medicine portfolio checks, ensuring accuracy and consistency across processes Qualifications • Bachelor’s degree (Pharmacy, Data, or related field preferred) • Minimum 2 years of experience in market research, pharmaceutical data, or related domain Skills & Competencies • Strong analytical and data validation skills • Proficiency in SQL and Excel (Python is an advantage) • Knowledge of drug classification systems (ATC, NFC, etc.) is highly preferred • Attention to detail and high level of accuracy • Ability to conduct research and resolve non-routine data issues independently • Strong adaptability and willingness to take on diverse tasks across team functions • Team-oriented mindset with ability to support multi-scope operations Nice-to-Have • Background in pharmacy or drug data management • Experience working with healthcare datasets or coding standards IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.• Assist with periodic review of study files for completeness.• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.• May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Qualifications• High School Diploma or equivalent  Req• 3-4 years administrative support experience.• r Equivalent combination of education, training and experience.• Minimum one year clinical research experience strongly preferred.• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of English language.• Effective time management and organizational skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.• Knowledge of applicable protocol requirements as provided in company training. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Summary Positions available on-site in Irving, TX and Fairfax, VA Job Summary The Clinical Nurse must be knowledgeable of standard research and oncology care practices. The Clinical Nurse advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care. Essential Duties and Responsibilities Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Protocol Compliance Adheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research. Complies with NEXT Oncology SOPs Participates in providing timely, informative, and accurate communication with the interdisciplinary team to ensure protocol compliance and timeliness of protocol-related procedures Collaborates with the PI, pharmacy, and other appropriate personnel to ensure proper use of and accountability for study drugs Informed Consent Identifies and intervenes to address barriers to effective informed consent discussions and decision making (e.g., literacy, capacity, language, distress, lack of time, therapeutic misconception) Describes and abides by institutional policy and processes for informed consent Assesses patient's understanding of the information provided during the informed consent process Ensures timely re-consenting as needed by the physician investigator. Confirms informed consent is obtained prior to performing any study specific tasks. Management of Clinical Trial Patients Provides complete patient assessment, including vital signs and pre-examination procedures Gathers and assess objective and subjective data from the patient Documents data and assessments accurately in the patient record Assists the providers in all aspects of the consultation, treatment, procedures, and follow-up care Records medical history and symptoms, completing documentation in the medical record Coordinates patient care, acting as a liaison with other departments and organizations Provides patient education before and after procedures, use of medical devices and equipment, and prescriptions Triage of calls for urgent appointments, referrals for patient consults and resting, insurance precertification, and documentation Educates the patient and family regarding clinical condition and/or disease process Ensures timely completion of protocol-required events and other requirements (e.g. pharmacokinetics or-dynamics, scans, study visits, QOL.) Assesses individual patients for physical, psychosocial, and financial factors that could impact adherence with study requirements and implement interventions as necessary Evaluates patient's adherence to and documentation of self-administered protocol agents and the return of such agents Collaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers Evaluates patient's adherence to and documentation of self-administered protocol agents and return of such agents Collaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers Ensures appropriate communication between clinical and research staff related to patient-specific care needs Ensures evidence-based symptom management as permitted by the protocol Patient health counseling and instruction, including meeting with families and caregivers Medication reconciliation, management, patient compliance, inventory, education Ensures regulatory compliance with OSHA guidelines, CLIA regulations, HIPAA medical privacy guidelines Documentation and Document Management Documents all patient encounters in the legal medical record per licensure and institutional requirements Obtains documents from outside providers or laboratories that are needed Assesses documentation or discrepancies and ensures that inaccurate or discrepant documentation is addressed in the medical record or other source documents Maintains the privacy and confidentiality of patient's source documents Other duties as assigned Required Education and Experience Current BLS and ACLS or obtained within 90 days of employment Current Registered Nursing License for the state the role is based in for RN's Oncology experience preferred Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $62,700.00 - $156,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job LocationOffice-based in Fairfax, VA Job SummaryThe Infusion Nurse must be knowledgeable of standard oncology care practices. The Infusion Nurse advocates for patient safety and protocol integrity, adheres to nursing standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care. Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Oncology Care Practices Demonstrates knowledge of age specific differences in the patient population including physiological and developmental differences unique to each group. Assess and monitors therapy of patients using appropriate technical skills under the direction and supervision of a physician. Assists physician with exams and procedures. Maintains efficient and appropriate patient 􀏐low. Demonstrates knowledge of reimbursement procedures and charge capture. Performs venipuncture, accesses implanted ports and maintains central venous access devices and alternate delivering systems. Documents all elements of care. Communicates all pertinent information and any interventions to the physician or mid-level provider. Serves as a resource person to the medical assistants and LPNs. Triages patient/family phone calls as needed and documents relevant information in the patient's chart. Assesses patient/family needs and provides teaching. Demonstrates awareness of community resources available to patients and assists with referrals if necessary. Follows OSHA guidelines when handling cytotoxic agents, biohazardous waste and any other material potentially infected with a blood borne pathogen. Maintains current knowledge of oncology nursing by participating in ongoing educational opportunities. Participates in professional development activities and maintain professional affiliations. Maintains patient confidentiality. Serves as mentor/preceptor and provides day to day guidance to less experienced nurses. Oncology Clinical Trial Practices Confirms informed consent is documented prior to performing any study specific tasks. Identifies patients who require increased nursing assessment and management in addition to the clinical trial requirements and collaborate with other members of the healthcare team to ensure patient safety. Provides patient education regarding required study procedures. Educates and evaluates patient’s adherence to and documentation of self-administered protocol agents, diaries, and return of such agents. Collaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers. Ensures appropriate communication between research and clinical staff related to patient-specific care needs. This may include telephone contact. Ensures evidence-based symptom management as permitted by the protocol. Administers investigational compounds and/or chemotherapy/biotherapy to patients according to the protocol and applicable regulations. Performs study-required procedures such as routine lab collection, study-specific sample collection, vital signs, and ECGs, according to the protocol-defined timeline. Records all study procedures performed including, but not limited to, vital signs, ECGs, blood draws, infusions, and infusion reactions. This may include collecting and documenting current medication lists. Required Education and Experience Current BLS and ACLS or obtained within 90 days of employment Current Registered Nursing License in the state the role is based in for RNs OCN preferred. IV and venous access device management skills Chemotherapy/Biotherapy administration experience Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $62,800.00 - $157,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewProvides high quality, timely development and on-time input to solutions for service delivery, managed services, or implementation oriented client projects. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams. Contributes to meeting client satisfaction objectives. Develops modules and low level designs while monitoring technical quality standards of onshore / offshore developers.Essential Functions Assists with the review and analysis of client requirements/problems and proposal development. Develops detailed requirements and design documentation and specifications. Performs basic quantitative or qualitative analyses to identify issues and develop solutions. Conducts customer trainings, requirement workshops and demos Assists team in design and structures of presentations. Develops a basic knowledge of software, services and consulting methodologies and the pharmaceutical/healthcare/life sciences industry. Develops an awareness of IQVIA technology solutions and how they would be utilized in client scenarios. Engagement based responsibilities are assigned and closely managed by Consultants, Engagement Managers or Principals. As a business analyst, validates the client deliverables and directs and reviews the work of an offshore project team. Qualifications Bachelor's Degree Req 3-5 years of related experience Req Works willingly and effectively with others in and across the organization to accomplish team goals. Familiarity with quality regulations in pharmaceutical/healthcare/life sciences industry. Prior experience with software implementations in pharmaceutical/healthcare/life sciences industry. Prior experience in authoring project documents such as business requirements document, technical requirements document, test scripts, etc. Ability to work on multiple projects, prioritize work and deliver on tight deadlines. Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline. Knowledge of consulting methodologies, tools, and techniques, related to functional area. Knowledge of current events and developments in the industry. Knowledge of quality management processes in pharmaceutical/healthcare/life sciences industry. Effective time management skills. Certifications: CCBA Certification (from IIBA) is a plus To be eligible for this position, you must reside in the same country/sales region where the job is located. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $67,500.00 - $170,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Summary Within IQVIA’s AI & Technology Solutions (ATS) organization, the Architecture & Standards (A&S) group defines “the IQVIA way” of building technology. The Enterprise Architecture (EA) function, operating within A&S, is responsible for translating business strategy and OKRs into scalable, standards‑driven architectures that reduce technical debt, enable reuse, and transform business processes. The Enterprise Architecture organization is seeking a Principal Enterprise Architect – AI & Agentic Solutions to define, govern, and evolve enterprise architecture strategy, standards, and roadmaps across a large, global technology landscape. This role plays a critical leadership position in shaping how AI and agentic capabilities are designed, governed, and adopted across IQVIA. The ideal candidate combines strategic vision with architectural rigor. They understand how emerging AI technologies can reshape research and data operations within a CRO environment while ensuring alignment with enterprise principles, governance, and compliance requirements. This leader balances innovation with pragmatism and can translate complex AI concepts into structured capabilities, reference architectures, and reusable patterns. The role requires comfort engaging across engineering, data science, and senior business stakeholders to deliver responsible, scalable, and standards‑driven enterprise AI solutions. Job Overview The Principal Enterprise Architect is accountable for co‑designing target‑state architectures and reference models for AI and agentic solutions, establishing enterprise guardrails (patterns, standards, and decision frameworks), and providing architectural oversight for priority initiatives. This role maintains a portfolio‑wide perspective of business and technical capabilities, identifying cross‑cutting needs and opportunities to consolidate platforms and services across application and data domains. The Architect champions interoperability and reuse through modern architectural approaches, cloud‑native delivery, and modern data platforms deployed on Azure and AWS. What success looks like: ·                     Published and broadly adopted AI and agent reference architectures Increased reuse of shared services, patterns, and templatesReduced duplication of AI implementations and development effortsFaster architecture reviews and approvals with fewer exceptionsImproved compliance readiness for regulated and high‑risk AI workloadsKey Responsibilities ·                     Define, maintain, and evolve enterprise reference architectures, standards, and reusable patterns for generative AI and agentic systems. Govern solution designs, including selection of appropriate technical components, ensuring delivery teams can adopt standards with minimal friction.Provide architectural oversight for major AI initiatives, guiding trade‑offs across security, compliance, scalability, cost, and time‑to‑value.Translate business strategies and OKRs into capability‑based roadmaps and target‑state architectures, avoiding project‑specific point solutions.Drive enterprise interoperability across systems and data domains by defining integration patterns and data exchange approaches aligned with enterprise standards.Partner with compliance, risk, and information security teams to ensure architectures align with global regulatory and quality expectations (e.g., GxP, GDPR, HIPAA, EU AI Act).Maintain enterprise capability models and architecture artifacts using EA tools (e.g., LeanIX, Ardoq, MEGA), mapping capabilities to processes, systems, products, outcomes, and key data domains.Identify opportunities to consolidate platforms and services across business units, quantifying investment implications and business benefits.Guide senior stakeholders through architectural options, trade‑offs, and investment decisions using clear, business‑focused narratives and models.Monitor AI, agentic, and life sciences technology trends; assess relevance and fit; and inform enterprise roadmaps, reference architectures, and innovation priorities.Mentor and influence architects and senior engineers to raise overall architecture maturity and adherence to enterprise standards.Required Qualifications ·                     10+ years of experience in enterprise or application architecture within large, complex organizations, including ownership of standards, roadmaps, and governance. Proven experience designing and scaling generative AI and agentic solutions, with a strong focus on reusable patterns and operationalization.Deep technical knowledge of generative AI and agentic concepts, including vector databases, RAG, tool‑use, MCP servers, HITL, evaluation frameworks, monitoring, observability, and platforms such as LangGraph.Strong cloud architecture experience on Azure and/or AWS, including modern data architectures (lakehouse, governance, cataloguing).Expertise in modern integration styles (API‑first, event‑driven, microservices) and the ability to codify them into enterprise standards and reference architectures.Exceptional communication, influence, and stakeholder management skills, including engagement with senior business, product, and technology leaders.Experience building business cases for modernization, rationalization, and platform consolidation initiatives.Preferred Qualifications ·                     Experience in healthcare or life sciences, with strong knowledge of the clinical trial lifecycle, real‑world evidence, or commercialization of clinical assets. Hands‑on partnership with CRO business teams, including study design, site activation and management, clinical operations, regulatory affairs, medical affairs and KOL engagement, real‑world safety and efficacy, pharmacovigilance, and EMR ecosystems.Proficiency with enterprise architecture tools (LeanIX, Ardoq, MEGA, or similar) and formal capability modeling methodologies.  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $118,100.00 - $328,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewDirect and manage the execution of the strategic, operational and financial delivery of required Site Activation activities, including but not limited to Site ID and Selection, Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company, scope of work and/or sponsor requirements. Essential Functions• Provides strategic planning and project oversight accelerating Site Activation through best in class project management to ensure fast site activation for patient enrollment, responsibilities may include;  Accountable for multiple regions.• Support and/or participate in pre-award/bid defense activities.• Oversee the execution of Start Up (including pre-award through Site Activation) and/or Lifecycle Maintenance for assigned projects in accordance with the agreed start up strategy, adhering to agreed project timelines and in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol, customer requirements, and internal policies.• Study Delivery Scope minimum expectations: accountable for multiple regions or Global SAM project oversight responsibilities.• Develop, implement and maintain the Site Activation Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required.• Collaborate with key stakeholders both internal and external, through effective communication and resolution management, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the Site Activation Management Plan.• Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents.• Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.• Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations. Identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the Site Activation Management Plan.• Provide ongoing updates and reporting to various levels of the organization, both study team and in some cases senior level colleagues.• Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.• Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required.• Adhere to quality standards, regulated and Company specific through the duration of the trial period.• Mentor and coach colleagues as required: mentor to Grade 140.• May take a lead role in developing long standing relationships with preferred IQVIA customers: Maintain and develop the customer relationship through study teamwork and support providing input to customer level processes and/or initiatives , attend Early Engagement Customer or Partnership Meetings if required.• Deliver presentations/training to clients, colleagues and professional bodies, as required.• Contribute to initiatives that affect positive change within the department and organization: support department and organizational initiatives. Qualifications• Bachelor's Degree Life sciences or related field Req• At least 5 years with 2 years of lead experience in a scientific or clinical environment. Req• Demonstrable experience in an international role; or equivalent combination of education, training and experience. Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $86,500.00 - $216,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Clinical FSP Business IQVIA clinical FSP business is unique.  Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients.  We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study. Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows.   Our managers understand the sponsors priorities and the individual aspects of each model.  Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development. Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’.  Additionally, IQVIA’s FSP business works with the Sponsors SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. What we Offer: Excellent salary and benefits packageCar allowanceWe invest in keeping our teams stable, so workload is consistentWe offer genuine career development opportunities for those who want to grow as part of the organisationWe give the chance to work on cutting edge medicines, right at the forefront of new medicine developmentRole Details: Working in partnership with a single-sponsorUsually allocated to 1-2 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)On site between 6 and 8 days per month, dependant on the sponsorAll CRAs and SCRAs are allocated a dedicated IQVIA Line ManagerPermanent employment contractFantastic work/life balanceSponsor model has reduced travel (approx. 30% or less) due to using ‘Fit for Purpose Monitoring’ which incorporates remote monitoring therefore there is less need for on-site visitsResponsibilities: Site management and monitoring activities across the countryWork with sites to adapt, drive and track subject recruitment planProvide protocol and study training to the assigned sitesCreate and maintain monitoring visit reports and action plansIf appropriate, co-monitor, train and mentor junior members of the team   Become part of our team. We believe in hiring the best talent in the industry. To become part of our team, you should: Have a degree in Life Sciences or have equivalent experience within a nursing background.Have at least 12 months of independent on-site monitoring experienceBe experienced in handling multiple protocols across a variety of drug indications with good time management skillsHave in depth GCP knowledgeBe flexible with the ability to travel nationwideHold a full driving licensePossess strong communication, written and presentation skills are a must (must have fluency in English)Whatever your career goals, we are here to ensure you get there!*Please note - this role is not eligible for VISA sponsorship*  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.