IQVIA

Job Overview Serve as the liaison between Records Management and user departments regarding Trial Master Files. Apply clinical research records management expertise to provide project-related assistance across multiple projects, sites, and project teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, Good Clinical Practice (GCP), and applicable regulatory requirements, while meeting quality and timeline metrics. May lead teams functionally, where assigned, including awareness of scope of work, budget, and available resources. Essential Functions Ensure project timelines are met and facilitate the orderly transfer, imaging, scanning, retention, and disposition of project-related and business records.Ensure all work is conducted in accordance with SOPs, policies, practices, Good Clinical Practice (GCP), and applicable regulatory requirements, and meets quality and timeline metrics.Coordinate the retrieval of records requested by users and prepare closed studies for transfer to final destinations within agreed timelines.Monitor filing accuracy and compliance with IQVIA or customer file plans and Standard Operating Procedures (SOPs).Conduct and manage imaging and scanning processes, and train staff on applicable imaging and scanning procedures.Maintain records center security to protect record integrity by ensuring compliance with SOPs.Interface with internal departments to support retrieval projects and ensure information needs are met.Train team members on records management tasks, policies, and procedures.Serve as the primary point of contact for internal and external clients.Coordinate the transfer, recall, and disposition of records to commercial records storage centers.Oversee the disposal of obsolete records and ensure efficient maintenance of records storage space, supplies, and equipment.Assist management with the implementation of strategic goals, plans, cost proposals, and resource projections for records management projects.May function as team leader for records management projects.Qualifications Bachelor’s degree in Records Management or a related field, or equivalent combination of education, training, and experience.Minimum of four (4) years of experience working in a technically related records management environment.Prior experience with Trial Master File (TMF) (oversight, review and/or reconciliation across clinical studies) is highly preferredStrong knowledge of applicable research and regulatory requirements, including International Council for Harmonization (ICH), Good Clinical Practice (GCP), and relevant local laws, regulations, and guidelines.Working knowledge of technology applications relevant to records management environments.Ability to identify and analyze problems, develop effective solutions, and make sound decisions.Demonstrated ability to manage multiple tasks and projects within defined timelines while balancing competing priorities.Strong attention to detail and ability to remain focused under pressure.Excellent organizational, planning, and decision-making skills.Strong written and verbal communication skills, including a solid command of the English language.Ability to establish and maintain effective working relationships with internal and external clients.Demonstrated ability to lead and guide others.This is a remote position open to candidates in the United States. 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 $47,400.00 - $118,600.00. 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.

Site Activation Specialist📍 Location: Athens, Greece - Hybrid🕒 Employment Type: Full-time  Job OverviewWe are seeking a highly organized and detail-oriented Site Activation Specialist to coordinate site activation activities across assigned studies. In this role, you will work under general supervision to ensure timely and compliant site start-up, in alignment with local and international regulations, SOPs, and project goals. You will collaborate closely with the Site Activation Manager (SAM), Project Management teams, and cross-functional stakeholders to drive efficient study start-up processes from feasibility through activation and maintenance. Key ResponsibilitiesPerform feasibility, site activation, and maintenance activities for investigative sites in assigned studies Support site start-up processes in compliance with regulatory requirements, SOPs, and study-specific guidelines Prepare, review, and manage site documentation, ensuring completeness, consistency, and accuracy Track and follow up on critical documents, including: Questionnaires Confidential Disclosure Agreements (CDAs) Regulatory and ethics submissions Informed Consent Forms (ICFs) Investigator Pack (IP) release documents Contract Negotiations & Budgeting Communicate status updates and document completion to internal teams and stakeholders Distribute finalized regulatory and study documents to sites and project team members Maintain and update internal systems, databases, tracking tools, timelines, and project plans with accurate information Collaborate effectively with cross-functional departments to ensure project timelines are met Qualifications🎓 Bachelor’s degree in Life Sciences or a related field ✅ Minimum of 4 years’ experience in a healthcare or clinical research environment (or equivalent combination of education, training, and experience) ✅ Strong understanding of clinical trial processes and site activation activities ✅ Ability to manage multiple tasks and timelines with attention to detail ✅ Proficient in working with internal systems, tracking tools, and documentation processes ✅ Strong organizational, analytical, and communication skills What We’re Looking ForA proactive and collaborative team player who thrives in a dynamic environment An individual contributor who can work independently under general supervision Someone comfortable handling non-routine tasks and applying judgment within established procedures Problem-solver with the ability to analyze issues and drive resolution What We Offer💼 Competitive compensation and benefits 🌍 Flexible working options (depending on location) 📈 Opportunities for professional growth and development 🤝 A collaborative, global, and inclusive work environment 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 OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.Role will be more locally focused as supposed to Global. Local knowledge is important in terms of submissions and contracts and start up. The role will be Hybrid and require in office visits weekly.   Essential FunctionsOversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan. Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizationsIdentify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. 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. Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information. May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients, colleagues and professional bodies, as required. May be involved in activities related to monthly study budget planning and reviews. QualificationsBachelor's Degree Life sciences or related field Req7 years’ relevant experience in a scientific or clinical environment including demonstrable experience in an international role. Thorough understanding of regulated clinical trial environment and in-depth knowledge of drug development process Demonstrated proficiency in using systems and technology to achieve work objectives Good regulatory and/or technical writing skills Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines In today’s world, continuing to grow and expand your skills is as important as ever. Discover career possibilities and chart your own path at IQVIA. The potential base pay range for this role, when annualized, is 34, 300 EUR - 66, 200 EUR. 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. Employee Referral Payment Standard Referral Bonus Plan 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.

Duties/Responsibilities: Act as signal detection and literature lead, or back-up lead to contribute to the conduct of ongoing literature safety surveillance for marketed and investigational products, evaluating      events of special interests as well as aggregate data reviewAuthor and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs and ACOs.Author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.Can serve as principal owner (molecule lead) for the molecule and have responsibility for completion of the deliverable and in compliance with all applicable Key performance indicators (KPI); Set-up and update products' signaling strategies, as approved by the customer’s Safety Strategy Lead. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterization of risks, as approved by the customer’s Safety Strategy Lead. Responsible for full documentation and tracking of signals.Ensuring the completion of molecule deliverables on time and liaise with portfolio clinical science scientists, service provider process leads and cross-functional stakeholders.  Distribution of molecule work within team consisting of molecule scientists, when necessary, coordinating support across molecules and disease areas when there are peaks and troughs in workload.End-to-end molecule work oversight and responsibility (i.e., ensuring consistent tracking of signals from detection to assessment to inclusion in aggregate reports).Ensuring an in-depth knowledge of the molecule and disease area within the service provider molecule team.Oversight and responsibility of quality-of molecule deliverables to the customer’s molecule team, with “hands-on” involvement, i.e., involved in authoring DSR conclusion, participating in SD/Lit meetings between service provider and customers.Responsible for resolution of issues on molecule deliverables (if necessary, in collaboration with service provider process lead).Participate in internal and external audits and inspections, as required.Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion to maintain compliance and documentedConduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members.Qualifications: Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance4-6 years of relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferredExcellent communication (written and verbal) skillsTeam workingEnglish – fluent (spoken, written)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 The Scheduler will schedule all routine and non-routine medical services with various local healthcare providers for an assigned patient population. In addition, the Scheduler will perform a variety of receptionist, clerical, record keeping and miscellaneous duties in support and care of services provided in an outpatient or inpatient medical setting. Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Daily confirmation of all on-site clinic and off-site appointments. Receive, screen and coordinate telephone calls from healthcare providers. Assist with maintaining and updating all provider addresses and phone numbers Receive incoming correspondence and review/forward to appropriate staff. Perform a variety of administrative duties including but not limited to answering phones; faxing and filing of confidential documents; and basic Internet and email utilization. Provide excellent customer service to all internal and external customers. Obtain patient information at the time of admission and assist in filling out forms, relevant documents, and case histories. Make and distribute daily schedules for doctors and staff. Maintain and update physician and patient data. Manage the front desk operations. Other duties as assigned. Required Education and Experience High School Diploma or GED Associate Degree and/or certificate program preferred Three years of medical clinic administrative or medical scheduling 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 IDS 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 $25,900.00 - $64,800.00. 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 OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Please note: for this role you must be based in the Netherlands. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.  Qualifications• Bachelor's Degree Degree in scientific discipline or health care is required.• At least 3 months of onsite monitoring experience is a must. • Dutch proficiency at C1 level or above is a must. • Written and verbal communication skills including good command of English language.• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good therapeutic and protocol knowledge as provided in company training. What we offer IQVIA provides a car (with private use) or a mobility allowance, fuel, insurance, maintenance, plus essential work equipment (laptop, and iPhone).Strong focus on professional growth, with access to learning and development resources, training programs, and opportunities to continuously build clinical and leadership expertise.Home office setup support and an annual wellness reimbursement for sport and wellbeing activities.Leave policy, including annual vacation days and additional year-end leave options.Comprehensive benefits package including pension plan, multiple insurance coverages, and optional partial reimbursement of supplementary health insurance, plus social and wellbeing activities.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 monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Please note: for this role you must be based in the Netherlands. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Qualifications• Bachelor's Degree Degree in scientific discipline or health care is required.• Requires at least 1 year of on-site monitoring experience as a CRA. • Dutch proficiency at C1 level or above is a must. • Written and verbal communication skills including good command of English language.• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good therapeutic and protocol knowledge as provided in company training. What we offer IQVIA provides a car (with private use) or a mobility allowance, fuel, insurance, maintenance, plus essential work equipment (laptop, and iPhone). Strong focus on professional growth, with access to learning and development resources, training programs, and opportunities to continuously build clinical and leadership expertise. Home office setup support and an annual wellness reimbursement for sport and wellbeing activities. Leave policy, including annual vacation days and additional year-end leave options. Comprehensive benefits package including pension plan, multiple insurance coverages, and optional partial reimbursement of supplementary health insurance, plus social and wellbeing activities. 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™ – 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. Komm in unser IQVIA-Team! Für ein spannendes Projekt im Bereich Impfstoffe suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt. Im Gebiet: Gummersbach   Das sind Deine Aufgaben: Durch die direkte Ansprache und intensive Betreuung ausgewählter Allgemeinmediziner, Internisten und Praktiker förderst Du die Verordnung Deines Impfstoff-Präparats und trägst so maßgeblich zum Unternehmenserfolg bei. In sehr eigenständiger Arbeitsweise bist du für den Aufbau und die Pflege langfristiger Beziehungen zu Ärzten und dem medizinischen Fachpersonal verantwortlich. Als Experte setzt Du auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Die Überwachung und das Management des Impfstoffbestands Deiner Kunden hast Du immer im Blick und stellst so eine kontinuierliche Verfügbarkeit und Versorgung sicher. Du erstellst eine eigenständige Routenplanung und pflegst Deine Besuche im CRM-System, inkl. Vor- und Nachbereitung. Das bringst Du mit: Du verfügst über eine naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG. Idealerweise verfügst Du über Erfahrung im Vertrieb von Impfstoffen bzw. hast eine hohe Bereitschaft und Begeisterung, Dich als Neueinsteiger in ein neues Aufgabengebiet einzuarbeiten. 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, runden Dein Profil ab. 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) 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 #Impfstoff #Chemie #Pharmareferent #75AMG #IQVIA #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.

Contract Negotiator -PolandWork Model: Hybrid Job OverviewWe are seeking a proactive and detail-oriented professional to support country-level activities related to site activation, start-up, and clinical trial agreements (CTAs). This role plays a key part in ensuring timely study initiation, compliance with regulations, and effective contract and budget management. You will work under moderate supervision as a developing individual contributor, supporting process improvements and collaborating cross-functionally to drive operational efficiency and high-quality outcomes. Key ResponsibilitiesSite Activation & Study Start-Up Act as the Single Point of Contact (SPOC) for investigative sites, Site Activation Managers (SAMs), Project Management teams, and other stakeholdersPerform feasibility, site identification, start-up, and site activation activities in compliance with applicable regulations, SOPs, and work instructionsPrepare, review, and distribute site documentation, ensuring completeness and accuracyMaintain accurate and up-to-date information in internal systems, databases, and tracking toolsTrack and follow up on regulatory and study documents, including:CDAs (Confidential Disclosure Agreements)SIFs (Site Information Forms)Ethics and regulatory submissionsInformed Consent Forms (ICFs)Investigator Pack (IP) release documentsMonitor project timelines, identify risks, and implement contingency plans where neededReview site performance metrics and provide feedback to managementProvide local expertise to SAMs and project teams during study planning and executionPerform quality control (QC) of documents provided by investigative sitesCommunicate progress updates and ensure alignment across cross-functional teamsContract & Budget Management Lead the negotiation and ongoing management of Clinical Trial Agreements (CTAs) with investigative sites and investigatorsCollaborate with Clinical and RSU teams to ensure timely site start-up and accurate forecasting of contract execution timelinesReview and negotiate site budgets in alignment with sponsor-provided calculations and study requirementsCommunicate and explain legal and financial terms to internal and external stakeholdersPrepare, review, and finalize CTA amendments based on sponsor requests and study guidelinesPerform QC of contracts, ensuring accuracy, completeness, and compliance with departmental standardsParticipate in project meetings to expedite contract negotiation and execution timelinesCreate, maintain, and organize contract documentation and filesSupport archiving of contracts for completed studiesQualifications & ExperienceBachelor’s degree in Life Sciences, Legal Studies, or a related field (required)Minimum 3 years of clinical research experience, or equivalent combination of education, training, and experienceExperience with site activation/start-up and CTA negotiation is highly preferredKnowledge of clinical trial systems is an advantageFamiliarity with regulatory documentation and clinical trial processesSkills & CompetenciesStrong communication and stakeholder management skillsProven negotiation and problem-solving abilitiesHigh attention to detail and strong organizational skillsAbility to manage multiple priorities in a fast-paced environmentCollaborative mindset and ability to work cross-functionallyA legal background is considered a plusWhat We’re Looking ForA motivated team player who can take ownership while working under moderate supervisionA professional who can identify process improvements and contribute to operational efficiencySomeone who can manage general challenges requiring a broader understanding of project and business needsWhy Join Us?You’ll be part of a dynamic and collaborative environment, contributing to impactful clinical research projects while developing your expertise in both site activation and contract management within a global organization. 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, when annualized, is 105.900,00 zł - 280.700,00 zł. 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.

Your Mission Be the biospecimen champion in global clinical trials! Drive strategy, ensure flawless sample collection and analysis, and guarantee data integrity. Your expertise powers breakthrough science and accelerates life-changing therapies. What You’ll Do Lead Biospecimen Strategy: Collaborate with clinical development teams to define and execute sample plans. Own the Lifecycle: Oversee collection, analysis, and data transfer for all biospecimens. Technical Leadership: Set up and manage labs for kit building, sample handling, and testing. Protocol Expertise: Provide input on sample-related sections in protocols and consents. Risk Management: Identify and escalate biospecimen-related risks; implement solutions. Training & Support: Develop lab manuals and training materials for clinical sites. Data Excellence: Ensure accurate data transfer and reconciliation with trial data managers. Close-Out Mastery: Manage sample disposition—storage, return, or disposal—at study end. Budget Oversight: Review lab proposals, forecast costs, and validate invoices. What You Bring Education: Bachelor’s degree in Life Sciences or related field. Experience: Strong background in clinical trials and biospecimen management. Skills That Shine: Deep knowledge of sample logistics and ethical considerations. Ability to collaborate across functions and geographies. Strong organizational and problem-solving skills. Technical expertise in lab operations and data integrity. Proficiency in SOP compliance and risk mitigation. Core Strengths ✅ Collaboration✅ Innovation✅ Ownership✅ Quality Focus✅ Communication Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. 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, when annualized, is 171.500,00 zł - 418.600,00 zł. 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.

Join us for an Open House at IQVIA Laboratories in Valencia, CA! On Monday, June 29, from 10:00 AM to 1:30 PM, IQVIA Laboratories will be opening its doors for a networking event and lab tour at our Valencia location. Whether you are actively exploring new opportunities or simply interested in learning more about our work, we invite you to join us at: IQVIA Laboratories28454 Livingston AveSanta Clarita, CA 91355 This is a great opportunity to connect with peers in the local bioanalytical community and learn more about our laboratory capabilities and operations. We are actively recruiting for our Laboratory and Biorepository teams, including opportunities such as: Associate ScientistLaboratory AssociateLaboratory AssistantOur hiring managers will be on-site to answer questions and discuss current and upcoming opportunities. To attend, please submit an application and attach your resume. If you have any questions, please contact: [email protected] *Please note that posted salary ranges and requirements may not reflect all positions being recruited for during the open house. 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 $35,900.00 - $74,800.00. 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.

Clinical Research Coordinator – Sioux Falls, SDWork Setup: On-siteSchedule: Part-time (24 hours per week) Shape the Future of Medicine with IQVIA! Are you passionate about advancing healthcare and improving patient outcomes? Join IQVIA as a Clinical Research Coordinator (CRC) and play a vital role in supporting clinical research studies that drive innovation. This hands-on position combines clinical procedures, recruitment activities, and compliance to ensure the highest standards of care. About IQVIAIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with top pharmaceutical, biotechnology, and medical device companies to accelerate innovation and improve lives. Our team blends scientific expertise with cutting-edge technology to deliver insights that transform clinical trials and healthcare worldwide. What You’ll DoPerform complex clinical procedures, including ECG, spirometry, sample collection, and vital signsPhlebotomy requiredCoordinate clinical research studies and ensure compliance with protocols and Good Clinical Practice (GCP)Prepare study materials, set up equipment, and manage logistical activitiesRecruit, screen, and orient volunteers while prioritizing their safety and well-beingCollect and accurately record clinical data in case report forms (CRFs)Collaborate with investigators and monitors to resolve queries and maintain data qualityAct as a volunteer advocate and maintain a safe environment in line with Health and Safety policiesFocus on Recruitment and Pre-ICF Activities: Pre-screening & recruitment support including chart reviews, referral management, and community outreachMake eCRF entries, corrections, and queriesInvestigator Site File maintenanceRegulatory experience would be a plusWhat We’re Looking ForHigh School Diploma or equivalent education and experienceMinimum 1 year of relevant clinical research experience (preferred)Working knowledge of clinical trials, GCP principles, and medical terminologyStrong attention to detail and ability to build effective working relationshipsAdvanced-level experience supporting site lead CRC with patient visits, data entry/query resolution, and prescreening physician referrals for eligibilityExperience working in both research and clinical settingsPlease note: This position is not eligible for sponsorship. #LI-CES #LI-DNP #LI-HCP #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 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 $35.00-$42.00 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.

Qualified Ultrasound Sonographer will be tasked with educating end users on a ultrasound machine used in hospital facilities and other healthcare facilities.You are responsible for end-user education and being a strong promoter of the product and company, you represent is highly valued. This Product Application Specialist role allows you to utilize your experience in a new way that does not involve direct patient care. Depending on your current schedule, this type of role can work in conjunction with your current position. Additionally, you will receive exposure to the ultrasound industry with the potential for long-term career growth in the field.Your primary focus will be in-servicing and education only; no sales responsibilities, and no bedside care.A desire to expand your talents in clinical education.Travel local, regionally and nationally to support customer needs.Appropriate PPE is provided to all employees prior to the start of assignments.Job Responsibilities:Provide peer-to-peer education and consultation to Ultrasound Sonographers and other healthcare staff in support of end-user education needs in the healthcare setting.Assess customer needs and assist with resolving issues stemming from lack of product knowledge or understanding of the particular product.Assist in the delivery of ultrasound-related in-service education to support key customers.Follow-up with key accounts and customers to assess unmet education and clinical needs as it relates to successful ultrasound machine implementation.Schedule:Per-diem position requiring travel and flexibility to work with your current schedule.2 weeks minimum of availability a month, more days preferred.Required Qualifications:Ultrasound Sonographer with POC experience, Cardiovascular or General Imaging US (Radiology)One of the following Credentials required: ARDMS, RDCS, CCI3+ years of experience as an Ultrasound SonographerMust be comfortable with basic software programsCustomer FocusedDemonstrate professional interpersonal skills, both oral and writtenDemonstrate excellent teaching skillsDuties may require compliance with client requirements that all those performing services on-site be fully vaccinatedPreferred Qualifications:Associate's Degree required, Bachelor's Degree preferredLeadership experience (manager, educator, preceptor) can be helpful but is not requiredBenefits:This position is not eligible for our Medical Benefits.IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities.Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  *Please note: Due to the nature of this role, it is not eligible for Visa sponsorship.#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 70 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.

【工作内容】1.    基于行业报告与文章，美化图表与制作PPT2.    为微信推文和活动物料提供设计平面设计支持3.    市场部的其他工作 【任职要求】1.    设计、广告等相关专业，大二大三或研究生优先2.    具有一定的design sense，prefer有相关实习经历的同学3.    尽快入职，每周到岗3-5天，可接受适当远程4.    熟练掌握PS、AI、MS office等软件 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 OverviewUnder general supervision, perform tasks at a country/region level associated with site activation activities in accordance with  applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities. Essential Functions• Under general supervision, perform feasibility,  site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Qualifications• Bachelor's Degree Life science or related field • Import permits (e.g., MFDS medical device confirmation, KMDIA process), customs clearance experience is preferred • Strong ability and willingness to quickly learn and adapt to assigned responsibilities • Effective communication skills in English with study teams • Prior experience as a Clinical Trial Assistant (CTA) or Study Coordinator (SC) is preferred 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.

Atividades Apoiar na gestão e controle de contratos com fornecedores e parceiros. Suportar na resolução de dúvidas de clientes relativo as soluções IQVIA. Realizar atividades administrativas relacionadas à organização de documentos, arquivos e relatórios. Monitorar e atualizar controles internos, garantindo conformidade com políticas e procedimentos. Auxiliar na elaboração de planilhas, indicadores e dashboards para acompanhamento de métricas. Apoiar processos de compras e pagamentos, garantindo prazos e documentação adequada. Contribuir para melhorias contínuas nos processos administrativos da área. Requisitos Ensino médio completo ou cursando graduação em Administração, Economia, Marketing ou áreas correlatas. Conhecimento básico em pacote Office (Excel, Word, PowerPoint). Organização, atenção aos detalhes e capacidade de trabalhar com prazos. Boa comunicação e habilidade para lidar com diferentes áreas e fornecedores. Disponibilidade para trabalhar no modelo híbrido em São Paulo/Capital. A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! 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 Under the direction and supervision of the Director of Data Management, this position is responsible for performing all data entry functions as they relate to the completion of case report forms, by entering study data collected by the research team into the Electronic Data Capture (EDC) system. Data entry personnel will also resolve all data queries. The position works closely with the research coordinators in support of all ongoing clinical studies. Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Oversee and manage the data entry from the source document to the case report form(CRF) Reviews patient records for completeness and accuracy Meets with sponsor/monitors to review data entry Serves as a backup to help coordinate and schedule monitoring visits Serves as a backup to provide support and information to monitors as necessary and as directed by supervisor(s) Timely resolution of data queries promptly to insure completeness of CRFs Assures that data entry remains current for all studies per SOP Complies with all applicable regulations, guidelines and procedures pertaining to dataloading, EDC and clinical research Identifies lab facilities used for studies so that lab certifications can be requested for study files Reviews and utilizes protocols as guides for study activities Communicates as needed with accounts receivable staff regarding submitted data Attends meetings and briefings regarding clinical studies as required Ability to assist in the guidance and training of less experienced staff Ability to maintain a positive attitude with the research team Maintain professional demeanor with sponsors, monitors, and auditors Remains current with all required training Performs other duties as assigned Knowledge, Skills and Abilities Working knowledge of clinical research Electronic Data Capture (EDC) systems Excellent interpersonal skills to deal effectively with research personnel Knowledge of medical terminology Knowledge of ICH GCP, FDA, OHRP, OSHA and HIPAA guidelines pertaining to clinical research Excellent organizational skills to independently manage workflow Ability to prioritize quickly and appropriately with minimal guidance Ability to multi-task Ability to work independently and function as part of a team Clear and concise verbal and written communications Required Education and Experience High School Diploma, Associate Degree and/or certificate program 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 $25,900.00 - $64,800.00. 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.

This is a fully on-site position in Salt Lake City, Utah Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. Why Avacare?At Avacare, CRCs wear more hats than in traditional research settings. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. What You’ll Gain:Broadened Skill Set: Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish. Professional Growth: Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training. Collaborative Culture: Be part of a supportive team that values initiative, adaptability, and continuous learning. Global Impact: Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO. Qualifications:Clinical Skills: Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens. Site Operations Knowledge: Solid understanding of site operations and the drug development process. Experience: CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants. CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants. Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management. Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools. Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish. 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 $36,600.00 - $91,300.00. 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.

Your Mission Be the biospecimen champion in global clinical trials! Drive strategy, ensure flawless sample collection and analysis, and guarantee data integrity. Your expertise powers breakthrough science and accelerates life-changing therapies. What You’ll Do Lead Biospecimen Strategy: Collaborate with clinical development teams to define and execute sample plans. Own the Lifecycle: Oversee collection, analysis, and data transfer for all biospecimens. Technical Leadership: Set up and manage labs for kit building, sample handling, and testing. Protocol Expertise: Provide input on sample-related sections in protocols and consents. Risk Management: Identify and escalate biospecimen-related risks; implement solutions. Training & Support: Develop lab manuals and training materials for clinical sites. Data Excellence: Ensure accurate data transfer and reconciliation with trial data managers. Close-Out Mastery: Manage sample disposition—storage, return, or disposal—at study end. Budget Oversight: Review lab proposals, forecast costs, and validate invoices. What You Bring Education: Bachelor’s degree in Life Sciences or related field. Experience: Strong background in clinical trials and biospecimen management. Skills That Shine: Deep knowledge of sample logistics and ethical considerations. Ability to collaborate across functions and geographies. Strong organizational and problem-solving skills. Technical expertise in lab operations and data integrity. Proficiency in SOP compliance and risk mitigation. Core Strengths ✅ Collaboration✅ Innovation✅ Ownership✅ Quality Focus✅ Communication Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. 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.

French Version ** Pour être éligible à ce poste, vous devez résider dans le même pays/la même région commerciale où se trouve l'emploi ** Location: Canada, Télétravail Description de poste interneIQVIA recrute afin d’élargir son équipe FSP dédiée en Données du monde réel (Real World Evidence – RWE), travaillant entièrement au sein de l’environnement d’une importante entreprise pharmaceutique. Le poste de programmeur en épidémiologie relève de notre équipe Real World Solutions et sera responsable de diriger le développement d’ensembles de données et de mener des analyses longitudinales pour des études observationnelles dans le domaine thérapeutique de la virologie, sous le portefeuille d’un client donné. Il est essentiel pour ce rôle de posséder une expérience démontrée ainsi qu’une maîtrise pratique de la recherche observationnelle utilisant des données de dossiers médicaux électroniques (DME/EMR) et des données de réclamations, de solides compétences en programmation statistique, une connaissance et une expérience appliquée de la conception d’études épidémiologiques, de la terminologie, de la constitution de cohortes et des mesures de résultats en RWE, ainsi qu’une expérience dans la gestion simultanée de plusieurs études et analyses complexes. Dans ce rôle, les personnes auront accès à des bases de données du monde réel et agiront à titre de gardiens des meilleures pratiques, normes et méthodologies du client liées à l’utilisation des données du monde réel (RWD). Responsabilités principalesDiriger le développement de jeux de données analytiques à partir du traitement des données brutes et effectuer les vérifications/nettoyages de données à l’aide de sources secondaires de données du monde réel, notamment les données de réclamations, de DME (EHR) et de laboratoire (p. ex. Optum, HealthVerity, TriNetX, IQVIA PharMetrics Plus)Diriger les analyses de faisabilité des sources de données du monde réel afin de caractériser les populations de patients, construire des cohortes et définir et valider les variables clés selon les objectifs des étudesRéaliser et assurer le contrôle qualité (QC) des analyses, incluant l’identification des codes diagnostiques et thérapeutiques et l’application de méthodes statistiques pour traiter les données censurées, les facteurs de confusion, les différences de temps-personne et les données manquantesCollaborer avec les épidémiologistes sur la conception des études et la méthodologie, ainsi que définir les spécifications pour les analyses statistiques descriptives et complexes (p. ex. analyses longitudinales, analyses de survie, modèles de régression, méthodes de scores de propension) dans des études utilisant des données RWD pour des questions de recherche en virologieDévelopper et assurer le contrôle qualité (QC) des TFL (tableaux, figures et listings) pour les protocoles, rapports et manuscrits utilisant des données du monde réel (p. ex. réclamations et DME)Soutenir la rédaction d’autres documents d’étude, notamment les protocoles, les plans d’analyse statistique et les rapports d’étudeCommuniquer les échéanciers, les rapports d’avancement et les résultats à l’équipe de projet et aux parties prenantes clésFournir une expertise technique en programmation, en statistiques et en épidémiologie, et proposer de manière autonome des solutions pour des projets complexesQualificationsMaîtrise en biostatistique, épidémiologie, recherche sur les résultats (Outcomes Research) ou dans un domaine connexe avec 5 à 8 ans d’expérience pertinente, ou doctorat (PhD) avec un minimum de 3 ans d’expérience pertinenteSolide expérience démontrée dans l’analyse de données du monde réel (RWD) utilisant des données de DME (EMR) et de réclamationsMaîtrise démontrée de la programmation statistique avancée utilisant SAS et/ou R, macros, SQLExpérience démontrée et maîtrise appliquée de la conception d’études RWE, de la terminologie, de la construction de cohortes et des méthodologies analytiquesExpérience préalable dans l’industrie pharmaceutiqueExcellentes compétences analytiques et en communication, avec un grand souci du détailCapacité à gérer efficacement et à prioriser plusieurs tâches et projets simultanémentEnglish Version **To be eligible for this position, you must reside in the same country/sales region where the job is located. ** Location: Canada, Home-Based IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company. Epidemiological Programmer role sits within our Real World Solutions team and will be responsible for leading development of datasets and conducting longitudinal analyses for observational studies in the virology therapeutic area under one client portfolio. It is important for this individual to have demonstrated experience and applied proficiency in observational research utilizing EMR and claims data, a strong statistical programming skillset, both knowledge and applied experience with epidemiological study design, terminology, cohort building, and RWE outcome measures, and experience managing multiple studies and complex analyses. In this role, individuals will have access to real-world databases and act as the stewards of the client’s best practices, standards, and methodologies underlying the use of real-world data (RWD). Essential Functions Lead development of analytic datasets through raw data processing and conduct data checks / cleaning using secondary real world data sources, including claims, EHR, and lab data (e.g. Optum, HealthVerity, TriNetX, IQVIA PharMetrics Plus)Lead the feasibility of real-world data sources to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives.Conduct and QC analyses, including identification of diagnosis and treatment codes and applying statistical methods to handle censored data, confounding, differing person-time, and missing dataCollaborate with epidemiologists on study design and methodology, as well as define specifications for descriptive and complex statistics (e.g. longitudinal analysis, survival analysis, regression models, propensity score methods) in studies using RWD for virology research questionsDevelop and QC TFLs for protocols/reports/manuscripts using RWD (e.g. claims and EHR)Support development of other study documents including protocols, statistical analysis plans, and study reportsCommunicate timelines, progress reports, and results to project team and key stakeholdersProvide technical, programming, statistical, and epidemiological expertise and independently bring project solutions to team for complex studiesQualifications Master's Degree in Biostatistics, Epidemiology, Outcomes Research or related field with 5-8 years relevant experience or PhD with 3 years relevant experience requiredStrong track record of analysis of RWD using EMR and claims dataDemonstrated proficiency in advanced statistical programming using SAS and/or R, macros, SQL requiredDemonstrated experience and applied proficiency of RWE study design, terminology, cohort building, and analytic methodologiesPrior pharmaceutical experienceExcellent analytic and communication skills with attention to detailAbility to effectively manage and prioritize multiple tasks and projectsIQVIA 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 $98,300.00 - $163,800.00. 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 $98,300.00 - $163,800.00. 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.

Role: Health Economics Consultant Location: Oeiras – Lisbon (Portugal) Permanent contract (full-time) As part of the local Real World Evidence team, the candidate will work from IQVIA Portugal’s office in Lisbon, with focus on local market access, supporting our Health Economics team. Typical projects include Health Technology Assessment (HTA) submissions, value dossier, systematic literature reviews, (network) meta-analyses, development (or adaptation) of economic models (e.g. budget impact, cost-effectiveness) and dissemination of the results (scientific articles, posters, etc). In this role, you will partner with leading clients across the pharmaceutical, biotechnology, and medical technology sectors. As part of a broader team, you will: Drive the execution of HTA submissions, value dossiers, literature reviews, meta-analyses and economic models, closely with a diverse range of peers (mainly using advanced Excel-VBAs and R)Manage projects across Health Economics business areas and the full breadth of therapeutic areas, ensuring on-time and on-budget delivery.Distil strategic insights from analytics that generate value for IQVIA’s clients.Develop tailored solutions to specific client problems as part of our team’s business development activities.Drive internal initiatives for the advancement of innovative methodological approaches.Collaborate with internal business areas and functions to deliver client services and support the development of new offerings.Mentor junior team members.Qualifications And Skills MSc in Economics / Mathematics / Statistics / Pharmacy or another relevant discipline with solid analytical backgroundPhD in Health Economics / Biostatistics / Epidemiology or related discipline will be considered a plusPrior relevant experience in Health Economics working in consultancy, CRO or pharmaceutical/biotech (relevant experience as post-graduate researcher may also be considered).Excellent MS Excel skills are required; VBA and R programming skills will also be valued.Strong time-management, organisational skills and attention to details are essential to the roleAttitude to work well as a team member and to build and manage relationships in a multi-cultural environment.Strong written and verbal communication skills with fluency in English and Portuguese.Eligibility to work in a hybrid regime.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.

Overview: Provides 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 • Supporting the design and build of new technology solutions including; understanding business needs, determining product specifications, production timetables, pricing, and time-integrated plans for product introduction; developing marketing strategies • Conducting market research; to understand business needs and generating product requirements • Managing internal and external cross functional stakeholders to support product development • Leveraging business experience and acumen in identifying strategic alternatives to client questions • Working in a team of like-minded professionals to create reports, presentations, workshops with client employees, management teams and other stakeholders, under the guidance our “the best on the business” team leaders • Developing broad knowledge of related consulting methodologies and pharmaceutical market through the delivery of consulting engagements and participation in formal and informal learning opportunities • Working independently and as part of a team • Assisting development and writing of proposals with senior support • Attending, supporting and presenting at client meetings • Contributing to learning, development and recruiting Qualifications • Bachelor's Degree Life Sciences / Economics / Business Pref Or • Master's Degree Life Sciences / Economics / Business Pref Or • Works willingly and effectively with others in and across the organization to accomplish team goals. 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 methods, tools and techniques, related to one’s functional area. Knowledge of current events and developments within an industry and major competitors. Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies. Effective time management skills. 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 $54,800.00 - $136,300.00. 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.

Sponsor requirement: Experience in Negotiating Clinical Trials Agreements and Budget Building in France Essential Functions Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations.  Responsible for delivery on established targets/measurements.Work with global teams to review and analyze contractual terms and conditions.  Assess legal and budget risks in conjunction with team support functions.  Partner with Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and drive resolution.  Escalate as appropriate.Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.Participate in discussions related to the development of site/investigator budgets aligned with fair market value.Manage the contract amendment lifecycle.Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.Assume responsibility for all aspects of legal document and metrics tracking.Provide support to review, authorize and/or understand aspects of site payments.  Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.Track all aspects of legal document and metrics.  Determine potential needs for contract amendments and manage amendment lifecycle.Qualifications Bachelor’s degree in related field3 years’ experience and/or equivalent competencies in legal/ pharmaceutical industry/clinical research.Excellent communication skills (both oral and written).Familiarity with healthcare compliance and other relevant guidanceFamiliarity with clinical research processes.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.

Overview IQVIA’s Financial Institutions Consulting (FIC) team advises investors (incl. private equity, venture capital, hedge funds) on biopharma and life sciences investments, including commercial due diligence, asset and target screening, portfolio company growth strategy and exit/divestment strategy. Successful candidates will have the opportunity to engage with clients on high-profile strategic investment decisions across a variety of transaction situations, business models and strategic issues. We operate in a multi-cultural, collaborative and fast-paced work environment, that is rich in development and growth. Role & Responsibilities As a Consultant within IQVIA’s FIC team, you will be responsible for delivering projects primarily in the areas of due diligence (buy- and sell-side), asset/portfolio/company valuation, asset screening and growth strategy Leverage consulting and/or transaction advisory experience, IQVIA information and expertise, and methodological know-how to deliver discrete workstreams / modules that address client / business questions. Solve strategic issues / diligence questions through a structured and evidence-driven approach, working both independently or in small teams as part of project workstreams Drive development of high-quality deliverables on a day-to-day basis, leveraging primary and secondary research approaches, including deriving analytical and qualitative insights to support assessments Serve as a core team member and workstream lead, including responsibility for presenting / communicating key project insights and recommendations to project management / leadership – ensuring engagement satisfaction and supporting long-term enhancement of client relationships Contribute to overall FIC team capabilities, including (but not limited to) the development of intellectual property, marketing materials, training, recruitment and proposal development About You Candidates interested in joining IQVIA FIC as a Consultant should have: Minimum of 4-5 years professional experience in strategy consulting, M&A/BD&L roles or within a financial institution (e.g. private equity, venture capital). Experience advising clients on commercial issues in the biopharma / life sciences industry and/or financial investors, including exposure to projects related to transactions / investments (due diligence, valuation, asset identification, growth strategy, forecasting) Experience working in multi-disciplined teams, including prior workstream oversight responsibilities Strong quantitative / analytical and qualitative research skillsets, supported by a problem solving mentality, keen eye for detail and critical thinking. Ability to drive primary/secondary research and analysis to assess business performance and synthesise findings into client deliverables Well-developed written and verbal communication skills including presentations and report writing Knowledge of key issues and current developments in the biopharma / life sciences industry Evidence of career progression in consulting and/or transaction advisory roles In addition to the skills and experience above, a Consultant should have: Bachelor’s degree or equivalent. MBA not required but a plus Fluency in English (spoken and written) A willingness and ability to travel (where required) Right to live and work in the recruiting country Benefits We work hard to prioritise the things that matter most to you. Visit our benefits page for information on everything from perks to well-being initiatives and career enhancement. 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, fort de ses 58 000 collaborateurs à travers le monde, est leader dans les informations (recueil, du traitement et de l’analyse des données de Santé), les technologies innovantes et les services de recherche clinique dans le secteur de la santé. Issue de la fusion entre IMS Health et Quintiles, IQVIA développe la science des données humaines en combinant la rigueur analytique et la précision des données pour répondre aux enjeux des évolutions du monde de la santé. IQVIA délivre des analyses décisionnelles uniques grâce au croisement de big data, de développements technologiques, de méthodologies d’analyses et d’une expertise pointue du domaine de la santé. Ces expertises permettent aux entreprises des sciences de la vie de repenser leur approche du développement clinique à la commercialisation de leurs produits et d’innover rapidement. Missions : Vous occupez un rôle hybride Commercial / Expert Solutions IQVIA au sein du département des Ventes. Vous devenez un expert de nos offres et solutions basées sur les « données patient » (Suivi du patient en pharmacie, EMRS, bases spécifiques à l’oncologie, bases de données publiques…) mais aussi sur l’analyse quantitative et la qualitative de l’activité promotionnelle de l’industrie pharmaceutiques et nos études ad’hoc. En collaboration avec l’ensemble des équipes alignées (KAM, Principal Consulting), vous agissez dans une logique d’account plan afin de maintenir et développer le chiffre d’affaire. Vous entretenez et développez les relations avec vos clients, vous êtes à l’écoute de leurs problématiques et proactif pour promouvoir les solutions IQVIA que vous représentez. Responsabilités :             Atteindre les objectifs commerciaux trimestriels fixés sur la vente des données et des solutionsÊtre en relation permanente avec les clients pour anticiper leurs besoins en optimisation commerciale et répondre rapidement à leurs attentesAssurer la satisfaction des clients par la pertinence des solutions proposées et par un suivi des projets menés pour eux, en s'appuyant sur ses propres compétences et sur celles des équipes compétentes au sein d’IQVIAAssurer l'évolution de son expertise pour répondre au mieux aux problématiques de ventes du client, transmettre son expertise aux autres collaborateurs d'IQVIATravailler en équipe avec les autres départements d'IQVIA, et notamment le consulting, les KAM/AM, le service client afin de proposer aux clients les solutions répondant à leurs besoinsIdentifier et développer des contacts clients dans les fonctions Marketing, Etudes, Market Access, BI.Conquérir de nouveaux clientsNégocier et conclure les contrats dans le respect de la politique commerciale IQVIAÊtre garant(e) de l'image et des valeurs d'IQVIA chez les clientsParticiper à la stratégie commerciale sur le parc clients : Account Plan, en relation avec les Key Account Managers et Principales Consulting alignésProfil : Formation : Bac+4/5 Commercial ou Scientifique, vous possédez une expertise en laboratoire ou dans des sociétés de prestation de service destinées aux fonctions marketing ou études des laboratoires Connaissances/compétences requises : Vous possédez une capacité à convaincre reconnue et du leadership.Vous êtes force de proposition et adaptable.Vous savez travailler en équipe et souhaitez relever un nouveau challenge.Connaissance des outils informatiques : Excel, PowerpointAnglais : bon niveauVous avez une expérience dans le milieu pharmaceutiqueLocalisation : Tour D2, 17 bis place des Reflets, 92400 Courbevoie, Esplanade de la Défense 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.