IQVIA

To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. In addition to leading LST(s), the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. MAIN RESPONSIBILITIES Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies Leads and optimises the performance of the Local Study Team(s) at country level ensuring compliance with Sponsor Procedural Documents, ICH-GCP and local regulations. Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality. Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks. Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in Sponsor clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head. Ensures timely preparation of local Master CSA (including site budget) and amendments as needed. Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enroll, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction). Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations. Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans. Reviews monitoring visit reports (as required and following Sponsor SOPs) and pro-actively advices the monitor(s) on study related matters. Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs. Proactively identifies risks and facilitates resolution of complex study problems and issues. Organises regular Local Study Team meetings on an agenda driven basis. Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders. Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead. Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary. Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the eTMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA. Provides input to process development and improvement. Provides regular information to Line Managers at country level on study and planned study milestones/key issues. Updates Line Managers about the performance of the CRAs/CSAs. Ensures that study activities at country level comply with local policies and code of ethics. Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. Ensures compliance with Sponsor´s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). Collaborates with local Medical Affairs team. Supports SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management. REQUIRED SKILLS AND QUALIFICATIONS Bachelor degree in related discipline, preferably in life science, or equivalent qualification. Minimum 3 years of experience in Development Operations (CRA, Sr CRA) or other related fields (Medical Affairs-led or Academic-led studies). Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and the Data Management Process. Excellent project management skills. Excellent ability to prioritize and handle multiple tasks, attention to details and negotiation skills. Excellent knowledge of spoken and written English and Italian language. Good ability to learn and to adapt to work with IT systems. Ability to travel nationally and internationally as required. 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 53 200,00 € - 79 800,00 €. 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.

Medical Science Liaison – Oncology (Community‑Based) - IQVIA in partnership with our client, Exelixis, are excited to announce that we are looking for Medical Science Liaisons to initiate scientific dialogue within the therapeutic area of oncology through scientific discussions with clinical physicians, staff and other stakeholders, on behalf of our client.  The Oncology Medical Science Liaison (MSL) is a field‑based scientific professional responsible for engaging healthcare professionals (HCPs) and advanced practice providers (APPs) in compliant, non‑promotional scientific exchange. This role is community‑focused and supports pre‑launch and early launch medical activities through disease‑state education, insight generation, and scientific engagement within community oncology settings. RESPONSIBILITIES Essential Functions Act as a scientific point of contact in the field for Exelixis Medical AffairsAppropriately engage oncology HCPs and APPs in compliant, fair‑balanced scientific exchangeDeliver scientific education and disease‑state discussions using approved materialsDevelop and maintain scientific relationships within assigned geographic territoryReport field intelligence, including insights on treatment landscape, scientific trends, and competitor activityProvide support to clinical development and operations activities, including site recommendations, initiation visits, and facilitation of scientific communicationParticipate in or support advisory boards in accordance with applicable guidelines and compliance standardsRepresent Exelixis at medical congresses and scientific meetings; provide timely session summariesServe as a scientific resource for cross‑functional partners within defined and approved boundariesMaintain up‑to‑date knowledge of relevant studies, compounds, disease states, and treatment pathwaysDemonstrate consistent execution excellence within assigned territory while supporting team objectivesContribute to business needs beyond assigned geography as requiredEnsure timely reporting of adverse events and product complaints in line with company and regulatory processesProject a professional image of the Company and act in accordance with applicable industry codes of conductPerform other duties as assignedSKILLS AND ABILITIES Strong verbal and written communication skillsAbility to engage healthcare professionals in credible and compliant scientific discussionsAbility to work independently while collaborating effectively within a matrix teamStrong organisational and time‑management skillsAbility to manage travel demands and territory prioritiesDemonstrated integrity and commitment to ethical and compliant conductProficiency in standard office software and customer relationship management systemsMINIMUM REQUIRED EDUCATION KNOWLEDGE AND EXPERIENCE Minimum Requirements: Bachelor’s degree (Life Sciences, BSN)2 years of relevant clinical, scientific, or healthcare‑facing experience in oncology.Relevant experience may include roles such as clinical practitioner, oncology nurse, clinical educator, clinical research, or other HCP‑facing scientific roles.Understanding of compliant, non‑promotional scientific exchange or experience working within regulated healthcare environments.Experience working within regulated, compliance‑driven healthcare or life sciences environmentsDemonstrated ability to manage territory activity, prioritise workload, and operate effectively in a fast‑paced, matrix environmentAbility to work independently in a field‑based, matrix organization.Understanding of the non‑promotional Medical Science Liaison role is requiredValid driver’s licenseFrequent domestic travel, up to 70%, including occasional evenings and weekendsPreferred qualifications and experience: Advanced scientific or clinical degree (e.g., PharmD, PhD, MD).Oncology‑specific certification (e.g., OCN®).Prior experience as a Medical Science Liaison or in a Medical Affairs role.Experience supporting oncology practices, particularly in community settings.Experience participating in scientific meetings, advisory boards, or investigator engagement.Knowledge of healthcare systems, particularly community oncology settings.Familiarity with applicable medical, legal, and regulatory requirements governing scientific exchange.#LI-CES 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 130,000-210,000 annually. 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 Overview The Junior Associate, Talent Acquisition Delivery Enablement role is responsible for collaborating with the Talent Acquisition team to ensure an efficient interview scheduling process, aiming to provide an excellent experience for both candidates and internal stakeholders. The ideal candidate should be proactive and dedicated to coordinating interviews effectively, with a focus on professionalism and customer service. The role is home-based in Phillipines and requires working second shift hours, supporting EMEA region. Essential Functions Own the end-to-end scheduling process for interviews, coordinating with candidates, hiring managers, and interviewers to facilitate timely and efficient interviews. Partner with Talent Acquisition and internal stakeholders as needed to ensure a smooth interview process. Develop strong and effective team relationships across Delivery Enablement, Talent Acquisition, Operations, and HR specialist functions, e.g., HR PSC, Finance, etc. Contribute to the continuous improvement of the interview process. Support ongoing or ad-hoc projects and initiative that support Delivery Enablement and the Talent Acquisition function. Provide guidance to line management and members of the HR team on recruiting matters as it pertains to the interview coordinator process. Provide reports and maintain data on coordinating activities as requested by management. Keep appraised of regional and local employment laws and regulations in order to ensure company compliance. Participate, as required, in activities and initiatives associated with change management involving reorganizations, mergers/acquisitions and transfers to ensure compliance with local legislation. Support new-hire onboarding to ensure smooth onboarding process. Qualifications Bachelor’s degree in Human Resources, Business Administration, Communication Studies, or related field preferred. 1+ years’ experience in an office environment or within an HR function preferred. Equivalent combination of education, training, and experience. Candidate must be fluent in English. Strong commitment to delivering high-quality customer service. Excellent organizational skills, attention to detail, and time management skills. Excellent communication skills, both verbal and written, with an emphasis on professionalism and confidentiality. Ability to work in a matrix environment and manage multiple priorities in a fast-paced environment. A proactive and solution-oriented mindset. Ability to establish and maintain effective working relationships with coworkers, managers, internal stakeholders, and candidates. Knowledge of Microsoft Office applications and HRIS applications, Workday and Rooster knowledge a plus. Knowledge of local and relevant employment laws and regulations. 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™ is The Human Data Science Company™, combining data, technology, advanced analytics, and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across the healthcare ecosystem and drive meaningful progress in life sciences.Team Overview IQVIA’s Financial Institutions Consulting (FIC) team advises investors (inc 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. Role & Responsibilities As an Associate Consultant within IQVIA's Financial Institutions Consulting (FIC) team, you will contribute to the delivery of consulting engagements focused on biopharma and life sciences investments. Projects typically include commercial due diligence (buy- and sell-side), asset and company valuation, asset screening, portfolio strategy, and growth strategy for investors and portfolio companies. Key responsibilities include: Support the delivery of projects by conducting analyses and developing insights that address client questions across due diligence, valuation, asset assessment, and growth strategy engagements.Leverage IQVIA data assets, industry expertise, and consulting methodologies to support project workstreams and deliver evidence-based recommendations.Conduct primary and secondary research, including expert interviews, market assessments, competitor analyses, forecasting, and evaluation of commercial opportunities.Analyze quantitative and qualitative data to assess market attractiveness, competitive dynamics, business performance, and investment opportunities.Translate research findings and analytical outputs into clear, actionable insights for internal teams and client presentations.Contribute to the development of high-quality client deliverables, including presentations, reports, and strategic recommendations.Participate in client meetings, helping to communicate project findings and support discussions with investors and senior stakeholders.Collaborate effectively within cross-functional and multicultural teams, demonstrating strong project ownership and accountability for assigned deliverables.Support business development activities, including proposal preparation, credential development, and market research.Contribute to broader FIC team initiatives such as intellectual property development, knowledge management, training, recruitment, and thought leadership activities.Continue developing expertise in consulting methodologies, transaction advisory, and key trends shaping the pharmaceutical and healthcare industries.About You Candidates interested in joining IQVIA FIC as an Associate Consultant should have: A Bachelor's, Master's, PhD, or equivalent degree in Life Sciences, Pharmacy, Medicine, Economics, Business, Finance, Engineering, or a related field.Approximately 2–4 years of professional experience in strategy consulting, transaction advisory, corporate development, business development & licensing (BD&L), or within a financial institution (e.g., private equity, venture capital, investment banking).Experience supporting projects related to commercial due diligence, transaction advisory, valuation, forecasting, asset identification, portfolio strategy, growth strategy, or other investment-related topics within healthcare and life sciences.Exposure to advising pharmaceutical, biotechnology, medical technology, healthcare services clients, and/or financial investors.Strong analytical and problem-solving capabilities, with experience interpreting quantitative and qualitative information and translating findings into business implications.Experience conducting market research, competitive assessments, commercial analyses, and/or forecasting exercises.Ability to work effectively in multi-disciplinary and fast-paced project teams, managing multiple priorities and delivering high-quality outputs under tight timelines.Strong written and verbal communication skills, including presentation development, business writing, and client-facing communication.A demonstrated interest in healthcare investing, life sciences innovation, and strategic transactions.Knowledge of key trends, market dynamics, and current developments within the pharmaceutical and healthcare sectors.Evidence of strong professional development and increasing responsibility within previous roles.In addition to the skills and experience above, an Associate 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. #CONAJD #LI-KS2 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.

Team Lead Software Development (m/w/d) hybrid Leipzig / Vollzeit (in Gleitzeit) Health System Services (HSS) wurde 1990 gegründet und ist einer der führenden Technologieanbieter und Dienstleister im deutschen Gesundheitsmarkt. Zu den Schwerpunkten unserer Tätigkeit gehören das Genehmigungs- und Abrechnungsmanagement, die Softwareentwicklung und -bereitstellung sowie Digitalisierungs- und Archivierungsleistungen für Krankenkassen. Als Team Lead Software Development (m/w/d) übernimmst Du die fachliche und disziplinarische Führung eines Entwicklerteams und gestaltest die Weiterentwicklung unserer zentralen Softwarelösungen aktiv mit. Dabei verbindest Du technische Expertise mit moderner Mitarbeiterführung und sorgst für stabile, zukunftsfähige Entwicklungsprozesse. Deine Aufgaben: Fachliche und disziplinarische Führung sowie Coaching eines agilen Softwareentwicklungsteams Unterstützung Deiner Mitarbeitenden in ihrer fachlichen und persönlichen Weiterentwicklung Steuerung und Organisation des Entwicklungsalltags nach Scrum-Methodik Sicherstellung von Entwicklungsstandards, Qualitätsvorgaben und Best Practices Verantwortung für die technische Planung und Weiterentwicklung teamrelevanter Softwarelösungen Mitwirkung bei Architekturentscheidungen und der Optimierung bestehender Systeme Analyse, Priorisierung und Umsetzung von Feature Requests sowie die Bearbeitung technischer Herausforderungen und Blocker Enge Zusammenarbeit mit Product Ownern sowie team- und bereichsübergreifenden Stakeholdern Verantwortung für datenbanknahe Prozesse sowie die Weiterentwicklung von Reporting- und Payment-Lösungen Sicherstellung einer hohen Systemstabilität sowie schnelle Fehleridentifikation und -behebung in geschäftskritischen Prozessen Dein Profil:Abgeschlossenes Studium der Informatik, Wirtschaftsinformatik oder einer vergleichbaren Fachrichtung bzw. eine vergleichbare Qualifikation Erfahrung in der professionellen Softwareentwicklung Erste oder mehrjährige Erfahrung in der fachlichen oder disziplinarischen Führung von Teams Gute Kenntnisse von Softwarearchitektur-Prinzipien und modernen Entwicklungsprozessen Fundierte Kenntnisse im Umgang mit SQL-Datenbanken und datenbankgestützten Anwendungen Erfahrung in den Bereichen Testautomatisierung und automatisierte Deployment-Prozesse Selbstständige, strukturierte und lösungsorientierte Arbeitsweise Ausgeprägte Kommunikations- und Organisationsfähigkeiten Verhandlungssichere Deutschkenntnisse in Wort und Schrift Werde Teil unseres Teams und gestalte gemeinsam mit uns die digitale Transformation im Gesundheitswesen. Das erwartet Dich: Flexible Arbeitszeiten im Gleitzeitmodell und hybrid (remote und im Office), full remote / anlassbezogen im Büro Faire Überstundenregelung mit Freizeitausgleich oder einer Vergütungsmöglichkeit mit 25% Überstundenzuschlag Mentoren-Programm während deiner gesamten Einarbeitungszeit Geregelte Feedbackschleifen in der Einarbeitung ("4 Tage, 4 Wochen, 4 Monate-Prinzip") und jährliche Entwicklungsgespräche Interne Entwicklungsmöglichkeiten innerhalb des IQVIA Konzerns Individuelle Weiterbildungen, unternehmensinterne Workshops, Teilnahme an Fachkonferenzen möglich Kantine mit subventioniertem Essen (Mittagsgericht ab 1,30 €) Kostenlose Kalt- und Heißgetränke und kostenfreies Obst Betriebliche Altersvorsorge Rabatte im Partner-Reisebüro Kostenfreie und anonyme Beratung zu gesundheitlichen, familiären und rechtlichen Anliegen über Talingo Vergünstigtes LVB-Jobticket Unternehmensevents, Weihnachtsfeiern und Teambuildings Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität. 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 OverviewResponsible for study design, edit specifications and system configurations. The Clinical database designer is accountable for associated quality and timely delivery of assigned study design components in collaboration with other project stakeholders. Essential Functions• Interprets the study protocol.• Design and update the eCRF.• Create and update Edit Specification Document.• Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)• Complete the Study Authorization Form and Trial Capacity Request Form (InForm)• Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting.  Attend and present comments at the Internal Design Review Meeting.• Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.• Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.• Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.• Escalate potential quality issues.• Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.• Reviews build timelines and provide input as applicable.• All responsibilities are essential job functions unless noted as nonessential (N). Qualifications• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req• 0-2 years of relevant core Technical designer experience and total exp being 5+ yrs.   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 OverviewResponsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from programming shared services perspective. Essential Functions• Interprets the study protocol.• Design and update the eCRF using third party or in house CDMS tools in alignment with industry standards like SDTM, CDASH as applicable.• Create and update Edit Specification Document.• Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)• Complete the Study Authorization Form and Trial Capacity Request Form (InForm)• Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting.  Attend and present comments at the Internal Design Review Meeting.  May lead Online Screen Review Meeting.• Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.• Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.• Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.• Escalate potential quality issues.• Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.• Reviews build timelines and provide input as applicable.• Reviews QIP for own projects, identify out of scope activities if any and inform relevant parties.• Responsible for multiple study design projects at the same time.• Might be working on projects across multiple platforms.• Identify areas for process improvements on an ongoing basis. Actively take part and contribute towards process improvement initiatives as assigned besides providing suggestions for continuous improvement of processes.• All responsibilities are essential job functions unless noted as nonessential (N). Qualifications• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology  Req• 2-4 years of relevant core Technical designer experience and total exp being 7+ yrs.   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. Bei IQVIA Contract Sales & Medical Solutions unterstützen Sie unsere Kunden darin, dem Gesundheitswesen neue Impulse zu geben. IQVIA hat die weltgrößte "Commercial Solution Organisation" die es ermöglicht, den Markteintritt und das Marketing von Produkten länderspezifisch, regional oder global mit rund 10.000 Mitarbeitern im Außendienst in mehr als 30 Ländern durch die Ansprache von Ärzten und Patienten zu optimieren. Für ein spannendes Projekt im Bereich Wundversorgung suchen wir Medizinprodukteberater (m/w/d) zum nächstmöglichen Zeitpunkt Im Gebiet: Neuwied, Bad Honnef, Betzdorf, Limburg   Das sind Deine Aufgaben: Du vertreibst hoch innovative Produkte aus dem Bereich der modernen Wundversorgung und Kompressionstherapie bei niedergelassenen Ärzt:innen und Pflegediensten. Du steigerst konstant den Marktanteil in Deinem Gebiet, erreichst die Umsatzziele und planst effiziente Besuche des bestehenden Kundenstammes und gewinnst Neukunden. Du führst Schulungen und Präsentationen durch und berätst Kunden zu moderner Wundversorgung und Kompressionstherapie. Das bringst Du mit: Als Medizinprodukteberater oder Direktverkäufer im Medizin-Sektor hast Du Dein verkäuferisches Talent bereits unter Beweis gestellt. Begeisterung, Spaß am Verkauf, klare Erfolgs- und Zielorientierung: Wenn Du Dich mit den aus unserer Sicht wichtigsten Voraussetzungen für den gemeinsamen Erfolg identifizieren kannst, bist Du bei uns genau richtig. 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. Als Medizinprodukteberater erwartet Dich eine spannende Herausforderung im Gesundheitsmarkt - dem wohl dynamischsten Markt überhaupt. Optimalerweise verfügst Du zusätzlich über eine Ausbildung im pflegerischen oder medizinischen Bereich oder bringst Fachwissen im Bereich Wundversorgung mit. 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 Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-DNP #LI-SS2 #Pharmaberater #Medizinprodukte #Apotheke #Apotheken-Außendienst #Wundversorgung #Krankenschwester #Krankenpfleger #Schwester #Pfleger #MPG #Außendienst Medizinprodukte 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.

 Attaché de recherche clinique II IQVIA est à la recherche d'un ARC II expérimenté en surveillance d'essais cliniques en oncologie. Ce poste, basé à domicile dans l'est du Canada, nécessite la maîtrise du français et de l'anglais. Aperçu du poste L'ARC II est responsable de la surveillance des essais cliniques de phase I à IV afin d'assurer la conformité aux protocoles, aux BPC/ICH et aux exigences réglementaires. Elle gère les activités des sites, du début à la clôture.Principales responsabilitésEffectuer les visites de sélection, d'initiation, de suivi et de clôture des sitesFormer le personnel des sites aux protocoles d'étude, aux systèmes EDC et aux exigences de l'étudeAssurer la qualité de la documentation source, l'intégrité des données et la résolution rapide des requêtesSuperviser la responsabilité des enquêteurs et la collecte des documents réglementairesÊtre l'interlocuteur principal du site et maintenir une communication régulièrePréparer les rapports de suivi conformément aux procédures opérationnelles standard (SOP) et aux échéanciersSoutenir les réunions des enquêteurs et collaborer avec les coordonnateurs principaux d'étude/ARCDiplômes et expérience Bilingue français-anglais (obligatoire)Baccalauréat requis. De préférence en sciences de la vie ou dans une discipline connexeUne combinaison équivalente de formation et d'expérience peut être acceptée au lieu du diplômeAu moins 1 an d'expérience en suivi sur place (requis)Disponibilité pour des déplacements à hauteur de 65 à 70 %Clinical Research Associate II IQVIA is seeking an experienced Clinical Research Associate II (CRA II) with oncology monitoring experience. This role is home‑based in Eastern Canada and requires fluency in both French and English. Overview The CRA II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from start-up through close-out. Key Responsibilities Conduct site selection, initiation, monitoring, and close-out visitsTrain site personnel on study protocols, EDC systems, and study requirementsEnsure high-quality source documentation, data integrity, and timely query resolutionOversee IP accountability and regulatory document collectionServe as the primary site contact and maintain regular communicationPrepare monitoring reports following Standard Operating Procedures and timelinesSupport investigator meetings and collaborate with CTMs/Lead CRAsQualifications Bilingual in French and English (Required).Bachelor’s Degree required. Preference in life sciences or related discipline.  Equivalent combination of education, training and experience may be accepted in lieu of degree.At least 1 year of onsite monitoring experience (Required)Ability to travel 65–70%IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $84,000.00 - $170,900.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $84,000.00 - $170,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.

About the RoleWe are seeking a highly motivated Senior Data Analytics Analyst to join our Data QA team. This role is responsible for ensuring the quality, accuracy, integrity, and reliability of enterprise data solutions through comprehensive testing, validation, and quality assurance processes. The successful candidate will lead Data QA activities across multiple projects, collaborate with business and technical stakeholders, and play a critical role in delivering high-quality data products, reports, dashboards, and analytics solutions.The ideal candidate combines strong analytical and testing skills with expertise in data validation, SQL, requirements analysis, and defect management. They will serve as a subject matter expert for Data Quality Assurance, helping establish testing standards, drive process improvements, and mentor junior team members.Major ResponsibilitiesAnalyze business, functional, software, and data requirements to ensure completeness, clarity, and testability.Develop, review, and maintain detailed test plans, test cases, test scripts, and test documentation.Perform manual and automated testing for data pipelines, databases, reporting solutions, dashboards, and analytics products.Validate data accuracy, completeness, consistency, integrity, and reconciliation across multiple systems and data sources.Identify, document, track, prioritize, and communicate defects while coordinating resolution efforts with development and data engineering teams.Execute regression testing, system integration testing (SIT), user acceptance testing (UAT), and end-to-end testing activities.Prepare and present testing results, quality metrics, risk assessments, and recommendations to project stakeholders.Lead and coordinate Data QA deliverables across multiple projects and initiatives.Partner with business users, analytics teams, data engineers, and technology teams to ensure successful implementation of data solutions.Establish, maintain, and promote QA standards, testing methodologies, and best practices across the organization.Support workload prioritization and resource coordination within the Data QA function.Act as the primary point of contact for Data QA risks, issues, escalations, and quality-related discussions.Drive continuous improvement initiatives to enhance testing efficiency, effectiveness, and overall data quality.Support data governance, audit, compliance, and regulatory requirements as needed.Mentor and provide guidance to junior QA and analytics team members.Perform additional duties as assigned.Required Qualifications & ExperienceBachelor’s degree in Computer Science, Information Systems, Data Analytics, Statistics, Engineering, Business, or a related field.3+ years of experience in software testing, data quality assurance, data validation, or analytics testing roles.Experience working with Amazon S3 and cloud-based data platforms.Strong understanding of software development lifecycle (SDLC), testing methodologies, and defect management processes.Experience testing data warehouses, databases, ETL/ELT processes, reporting platforms, and analytics solutions.Experience creating and executing test plans, test cases, and test scripts.Strong analytical and problem-solving skills with excellent attention to detail.Ability to manage multiple priorities and deliverables in a fast-paced environment.Excellent verbal and written communication skills.Proven ability to collaborate effectively across cross-functional teams and stakeholders.Good to HaveKnowledge of US Healthcare data, processes, and reporting requirements.Understanding of HIPAA regulations and healthcare compliance standards.Experience with data governance and audit support activities.Exposure to automated testing frameworks and tools.Experience mentoring junior analystsIQVIA 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.

This is a fully on-site position in Jefferson City, MO 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 $44,300.00 - $110,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA™ – 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 Gesundheits-versorgung zu erzielen. Werde Teil unserer Community von rund 90.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welcher Rolle Du bei IQVIA einsteigst, es erwartet Dich ein offenes, innovationsfreudiges Umfeld, indem Du viel bewegen kannst. Finde heraus, wie Du Deine Talente und Deine Leidenschaften bei IQVIA einbringen kannst. Aktuelle und umfassende Marktinformationen sowie hochwertige Daten, die wir weltweit gemeinsam mit Partnern im Gesundheitsmarkt erheben, sind ein zentraler Erfolgsfaktor für IQVIA. Neben Pharmagroßhändlern, Apotheken und Ärzten spielen insbesondere Krankenhäuser eine entscheidende Rolle als Datenpartner. Der Schwerpunkt dieser Position liegt auf der Betreuung und Unterstützung unserer Krankenhauspartner. In dieser Rolle übernehmen Sie die Verantwortung für den gezielten Ausbau und die Weiterentwicklung unserer Beziehungen im Hospital‑Umfeld. Ziel ist es, unser bestehendes Portfolio bei unseren Krankenhauspartnern weiter zu stärken, neue Lösungen zu entwickeln und diese erfolgreich zu etablieren. Zur Verstärkung unseres Teams suchen wir zum nächstmöglichen Zeitpunkt einen motivierten Hospital Account & Solution Manager Supplier (m/w/d) mit ganzheitlichem Interesse an der Pharma‑ und Healthcare‑Industrie. Deine Aufgaben: Du hast Spaß am Netzwerken und daran, unsere Lösungen auf Messen, lokalen Events, in Arbeitskreisen sowie über soziale Medien sichtbar zu machen Dabei knüpfst du neue Kontakte und entwickelst bestehende Netzwerke kontinuierlich weiter Du schulst unsere Partner in der Handhabung unserer Tools, führst Workshops durch, begleitest Messen und stehst bei technischen sowie inhaltlichen Fragen für unsere Partner‑Häuser zur Verfügung Du treibst die Weiterentwicklung bestehender Lösungen voran, identifizierst Optimierungspotenziale und beobachtest den Markt hinsichtlich neuer Trends und Lösungen im Healthcare‑Sektor Digitale Tools sowie der enge, bereichsübergreifende Austausch mit anderen Teams unterstützen dich dabei In der Umsetzung übernimmst du eigenverantwortlich die Projektleitung, behältst Termine im Blick, koordinierst interdisziplinäre Projektteams und stellst einen reibungslosen Projektfortschritt sowie die erfolgreiche Integration und Inbetriebnahme neuer Lösungen und Prozesse sicher Dein Profil: Du verfügst über eine abgeschlossene Berufsausbildung oder ein abgeschlossenes Studium im Gesundheitswesen oder in einem MINT‑nahen Studiengang (z. B. Informatik, Biologie oder Naturwissenschaften) und bringst Interesse an digitalen Lösungen im Krankenhausumfeld mit Du bringst mehrjährige Erfahrung im Vertrieb mit – idealerweise im Umfeld von Software‑, oder datenbasierten Lösungen für Krankenhäuser Du kannst nachweisliche Erfolge beim Beraten, Positionieren oder Verkaufen von Softwarelösungen im Krankenhausumfeld vorweisen Du verstehst die Anforderungen und Entscheidungsprozesse von Krankenhäusern und kannst komplexe Lösungen verständlich und überzeugend präsentieren Du hast Freude daran, aktiv Netzwerke aufzubauen und zu pflegen – sowohl im persönlichen Austausch als auch über soziale Medien Du trittst sicher und überzeugend auf, präsentierst leidenschaftlich gerne und begeisterst Kunden für Lösungen und Mehrwerte Ein hohes Maß an Eigeninitiative, Kommunikationsstärke sowie eine ausgeprägte Kunden‑ und Abschlussorientierung runden dein Profil ab Was Dich erwartet: Abwechslungsreiche Tätigkeiten mit viel persönlichem Austausch und Kontakt zu Menschen aus unterschiedlichsten Bereichen im Klinikumfeld Direkte und enge Zusammenarbeit mit den Softwareentwicklern im eigenen Team für schnelle Abstimmungen und effiziente Lösungen Attraktives Gehaltspaket inklusive Dienstwagen Aktive Mitarbeit an bereichsübergreifenden Projekten zur Weiterentwicklung und Gestaltung unseres Angebotsportfolios Flexible Arbeitszeitmodelle sowie die Möglichkeit zum Homeoffice für eine optimale Work‑Life‑Balance Wir freuen uns auf Deine vollständige Bewerbung mit Angabe des frühestmöglichen Eintrittstermins und Deiner Gehaltsvorstellung – bitte vorzugsweise online IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview:Provides complex Data Center support to meet uptime goals.  Serves as Data Center technical subject matter expertise and hands on participation to maintain, troubleshoot and manage Data Center Systems. Essential Functions: Manages the installation, maintenance, and upgrades of internal and external computer hardware systems used for designing, developing, and deploying company products.Works with Infrastructure and Business services to provision and setup environments.Assist with designs of automation scripts and best practice processes to minimize the human intervention required for Data Center Environments.Proposes and guides implementation of systems and enhancements that will improve the reliability and performance of the Data Center Environment.Monitors usage and performance and utilizes all standard tool sets for management of all aspects of the Data Center environment.Responds to production issues escalated by client and support teams –requires a deep understanding of the Data Center functionality, architecture, and design, as well as production hardware infrastructure design.Trains personnel on Data Center Processes and systems.Works with Service Providers to ensure that the operational aspects of a Data Center are working properly.Qualifications: Bachelor's Degree with 5 years of related experience Req or Master's Degree with 3 years of related experienceEquivalent experience can be substituted for degree ReqIncumbent must have in-depth knowledge of large-scale enterprise Data Center Operation platforms. Must be comfortable working within on Prem, distributed, and hybrid Data Center environments.Must demonstrate ability to combine metrics, events, and traces into a holistic IT Operation system.Must have good knowledge of Data Center Facilities, server, network, virtualization, cloud, and container technologies.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 Posting Title- Clinical Trial Operations Specialist (CTOS)Location: Home-based in the U.S.Job OverviewProvide operational support and coordination for global clinical trials, ensuring efficient trial execution from planning through close-out. Responsible for managing trial-related documentation, systems, communication, and logistics in compliance with SOPs, ICH-GCP, and regulatory requirements, while meeting quality and timeline objectives. Essential FunctionsPlan, coordinate, and execute clinical trial activities across regions in compliance with ICH-GCP, ensuring timely and high-quality delivery.Maintain and oversee trial documentation (e.g., ISF, TMF, submissions), ensuring completeness, accuracy, timeliness and audit readiness.Collaborate with global and regional stakeholders, vendors, and trial teams to ensure seamless trial conduct and communication.Manage and maintain clinical trial systems, databases, and tracking tools ensuring data accuracy.Prepare and distribute project plans, status updates, reports, and presentation materials.Monitor trial progress, budgets, and system data, identifying risks and implementing corrective actions as needed.Coordinate documentation workflows, regulatory submissions, and communication with authorities and regional teams.Support reporting, trial close-out activities, and preparation of key deliverables (e.g., CTR appendices).Coordinate logistics for trial meetings, materials, and supplies.Contribute to quality oversight, inspection readiness, and best practices in clinical trial conduct.Act as a key point of contact for trial-related systems, documentation, and operational queries.QualificationsUniversity degree qualified and/or comparable professional education with at least 3+ years’ experience in clinical trial operations or project coordination.Exceptional communication and stakeholder management skills.Strong knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Excellent organizational and problem-solving skills with ability to work independently, prioritize tasks, and manage projects in a complex international environment.Detail-oriented with strong commitment to quality and compliance.Proficiency in MS Office and clinical trial systems/tools.Fluent in written and spoken English.#LI-Remote #LI-NITINMAHAJAN 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 $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Position Summary We are seeking a Principal Statistical Programmer to provide full end‑to‑end statistical programming support across clinical development programs. This role requires deep technical expertise, leadership, and hands‑on delivery, covering SDTM, ADaM, TLF development, and regulatory submission support. The Principal Statistical Programmer will serve as a subject matter expert, ensure high‑quality deliverables, and contribute to programming standards and best practices. Key Responsibilities Provide end‑to‑end statistical programming support for clinical studies from study setup through submission Lead and perform development and validation of: SDTM datasets ADaM datasets Tables, Listings, and Figures (TLFs) Ensure all deliverables are compliant with CDISC standards and regulatory requirements Support regulatory submissions (e.g., FDA, EMA), including define.xml, submission‑ready datasets, and reviewer’s guides Serve as a Principal‑level programmer, providing technical leadership and guidance to other programmers as needed Contribute to and help maintain programming standards, macros, and validation processes Review and approve programming deliverables to ensure accuracy, consistency, and quality Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams Proactively identify risks and propose efficient, compliant solutions within timelines Required Qualifications Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or related field Extensive experience as a statistical programmer, with demonstrated Principal‑level responsibilities Strong hands‑on experience with: SDTM and ADaM dataset development TLF programming Regulatory submission deliverables Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros In‑depth knowledge of CDISC standards, regulatory guidelines, and submission requirements Proven ability to manage complex studies independently from start to finish 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 $98,200.00 - $273,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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

** This is a pipeline job posting to gather resumes for a future opportunity ** Sales Representative About the Role:We are seeking a motivated and results-driven Pharmaceutical Sales Representative to join our team. In this role, you will be responsible for driving volume and market share growth for assigned pharmaceutical products within a designated territory. You will build strong relationships with healthcare professionals and deliver impactful sales presentations in an office-based setting. Key Responsibilities Include: Generating volume and market share growth for assigned pharmaceutical products within a specific geographic area. Selling presentations to physicians and other health care professionals, primarily in an office-based setting. Developing an understanding of the issues and opportunities unique to the geography, particularly in managed health care. Manage allocated resources (samples, promotional and educational materials) to maximize return within regulatory and ethical guidelines. Maintains accountability for all pharmaceutical samples in accordance with FDA and PDMA guidelines. Utilize the sales automation system to document call and program activity. Complete initial and ongoing product and development training as required.Requirements: BA/BS requiredPreferred: Minimum of 2 years business-to-business outside sales experience with demonstrated record of impact preferred. 1-2 years of Pharmaceutical Sales experience with demonstrated record of impact preferredEstablished relationships within targeted geography.Key Competencies: Sales ability/persuasiveness, use of appropriate interpersonal style and communication methods to facilitate an acceptance of an idea, plan, activity or product from targeted customers.Establishes account plans based on customer needs and business priorities.Establishes method for monitoring progress to goals.Must set high goals or standards of performance, self-starter, able to work independently.Must demonstrate ability to influence events to achieve goals and take actions beyond what is required in being proactive.Must be able to utilize resources and create a positive/professional impression, commanding attention and respect, displaying confidence.Ability to maintain effectiveness in varying environments and with different tasks, responsibilities and people is key.Must express ideas effectively in individual and group situations, adjusting to the characteristics or needs of the target audienceWhether you're educating prescribers, supporting patients, or engaging with physicians, you'll help demonstrate product value and contribute to real-world medical breakthroughs. Explore your potential and help shape a healthier future with IQVIA. #LI-CES 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 $90-115,000 annually. 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.

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

Job Overview We are seeking a highly motivated candidate to join our Key Account Management team. This is a hybrid role based in Budapest. As a Key Account Manager, you will have the opportunity to contribute to the sales efforts for IQVIA products and services through building client relationships. Your main goal will be to achieve assigned revenue targets and ensure high customer satisfaction. Collaboration will be key as you work closely with the client service team and internal senior management team to deliver comprehensive solutions to clients. You will act as a trusted advisor, understanding and addressing clients' needs by proposing multiple fit-for-need solutions. Key responsibilities: Understands the key priorities of the client to achieve or exceed the assigned revenue and growth goal in assigned accounts or sales territory. Based on long term relationship with client, acts as advisor on marketing, market research, sales management, industry issues, trends and IQVIA product, consulting and service capabilities. Anticipates clients’ needs and, in collaboration with IQVIA marketing, sales specialists, consulting and client service, develops and presents proposed solutions to client's complex business issues. Identifies and leads the pursuit of the targeted new business and contract expansion opportunities within assigned accounts. Interfaces with marketing, market research, sales management and/or IT at the manager level in existing and prospective clients. Represents the company to the client and the client to the company in all sales related activities. Monitors client satisfaction with contracted deliverables and works with sales management team and Client Service’s management to achieve and maintain a high level of customer satisfaction. Participates in contract renewal efforts on large contracts as required. May work with global and regional account management in the pursuit of multi-country opportunities. Key requirements: Bachelor's or Master’s degree in business, management or equivalent 3-5+ years of relevant sales or account management experience and/or solution sales management experience (preferred) B2B experience is a must Fluency in Hungarian and English language Strong teamwork and collaboration skills Pharma or Technology industry required Why Join Us? Be part of a publicly traded global leader in the healthcare market and becoming an expert in the field Have an opportunity to fast track your career growth and have great client exposure Collaborate in a team with a supportive and dynamic atmosphere Work in an international environment with daily collaboration across Europe Be rewarded with an attractive salary and package 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.

Help bring clarity, structure, and predictability to regulatory project delivery. At IQVIA, we're advancing healthcare by helping life sciences organizations navigate complex regulatory environments and bring therapies to patients faster. We're looking for a highly organized and detail-oriented Project Analyst to support the successful delivery of regulatory projects and programs across our Global Regulatory Affairs team. In this role, you'll work closely with Project Managers, delivery teams, finance partners, and stakeholders to ensure projects remain on track, risks are visible, reporting is accurate, and governance standards are consistently maintained. If you enjoy turning data into insight, coordinating across functions, and creating structure in fast-moving environments, we'd love to hear from you. What You'll DoAs a Project Analyst, you will play a key role in supporting project planning, tracking, reporting, and operational governance by: Supporting project setup, planning, and mobilization activitiesMaintaining project plans, schedules, trackers, and delivery dashboardsMonitoring milestones, action items, risks, issues, and dependenciesPartnering with project finance stakeholders to support effort tracking, forecasting, revenue reconciliation, billing activities, and scope change managementPreparing project status reports, metrics, and materials for internal and client-facing meetingsEnsuring project documentation remains complete, accurate, and audit-readyCoordinating onboarding and offboarding activities for project team membersIdentifying data inconsistencies, emerging risks, and operational issues, escalating concerns proactivelySupporting the continuous improvement and standardization of project management tools, templates, and reporting practicesRequired Skills & Experience2–5 years of experience in project support, project coordination, operational delivery, PMO, or similar environmentsStrong organizational skills and ability to manage multiple priorities simultaneouslyHigh attention to detail and commitment to data accuracyExperience maintaining project plans, trackers, reports, and documentationStrong analytical and problem-solving capabilitiesEffective communication and stakeholder coordination skillsAbility to work successfully within cross-functional and matrixed teamsProficiency with project reporting and collaboration toolsPreferredExperience within Regulatory Affairs, life sciences, healthcare, clinical research, or pharmaceutical environmentsExposure to project governance, financial tracking, forecasting, or operational reportingInterest in developing a career in project management and delivery leadershipIn this role, you'll help create: Accurate and timely project reporting that supports informed decision-makingStrong project governance and compliance with delivery processesBetter visibility of risks, issues, and project performanceReduced administrative burden for Project Managers and technical teamsImproved forecasting, financial control, and operational efficiencyConsistent, scalable delivery practices that support business growthWhy IQVIA?IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make a bigger impact on healthcare. 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 23 500,00 € - 35 300,00 €. 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.

Medical Science Liaison – Oncology (Community‑Based) - IQVIA in partnership with our client, Exelixis, are excited to announce that we are looking for Medical Science Liaisons to initiate scientific dialogue within the therapeutic area of oncology through scientific discussions with clinical physicians, staff and other stakeholders, on behalf of our client.  The Oncology Medical Science Liaison (MSL) is a field‑based scientific professional responsible for engaging healthcare professionals (HCPs) and advanced practice providers (APPs) in compliant, non‑promotional scientific exchange. This role is community‑focused and supports pre‑launch and early launch medical activities through disease‑state education, insight generation, and scientific engagement within community oncology settings. RESPONSIBILITIES Essential Functions Act as a scientific point of contact in the field for Exelixis Medical AffairsAppropriately engage oncology HCPs and APPs in compliant, fair‑balanced scientific exchangeDeliver scientific education and disease‑state discussions using approved materialsDevelop and maintain scientific relationships within assigned geographic territoryReport field intelligence, including insights on treatment landscape, scientific trends, and competitor activityProvide support to clinical development and operations activities, including site recommendations, initiation visits, and facilitation of scientific communicationParticipate in or support advisory boards in accordance with applicable guidelines and compliance standardsRepresent Exelixis at medical congresses and scientific meetings; provide timely session summariesServe as a scientific resource for cross‑functional partners within defined and approved boundariesMaintain up‑to‑date knowledge of relevant studies, compounds, disease states, and treatment pathwaysDemonstrate consistent execution excellence within assigned territory while supporting team objectivesContribute to business needs beyond assigned geography as requiredEnsure timely reporting of adverse events and product complaints in line with company and regulatory processesProject a professional image of the Company and act in accordance with applicable industry codes of conductPerform other duties as assignedSKILLS AND ABILITIES Strong verbal and written communication skillsAbility to engage healthcare professionals in credible and compliant scientific discussionsAbility to work independently while collaborating effectively within a matrix teamStrong organisational and time‑management skillsAbility to manage travel demands and territory prioritiesDemonstrated integrity and commitment to ethical and compliant conductProficiency in standard office software and customer relationship management systemsMINIMUM REQUIRED EDUCATION KNOWLEDGE AND EXPERIENCE Minimum Requirements: Bachelor’s degree (Life Sciences, BSN)2 years of relevant clinical, scientific, or healthcare‑facing experience in oncology.Relevant experience may include roles such as clinical practitioner, oncology nurse, clinical educator, clinical research, or other HCP‑facing scientific roles.Understanding of compliant, non‑promotional scientific exchange or experience working within regulated healthcare environments.Experience working within regulated, compliance‑driven healthcare or life sciences environmentsDemonstrated ability to manage territory activity, prioritise workload, and operate effectively in a fast‑paced, matrix environmentAbility to work independently in a field‑based, matrix organization.Understanding of the non‑promotional Medical Science Liaison role is requiredValid driver’s licenseFrequent domestic travel, up to 70%, including occasional evenings and weekendsPreferred qualifications and experience: Advanced scientific or clinical degree (e.g., PharmD, PhD, MD).Oncology‑specific certification (e.g., OCN®).Prior experience as a Medical Science Liaison or in a Medical Affairs role.Experience supporting oncology practices, particularly in community settings.Experience participating in scientific meetings, advisory boards, or investigator engagement.Knowledge of healthcare systems, particularly community oncology settings.Familiarity with applicable medical, legal, and regulatory requirements governing scientific exchange.#LI-CES 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 130,000-210,000 annually. 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.

Location: Colombia, Mexico (Hybrid)Employment Type: Full‑time About the role We are expanding our LATAM near‑shore team to support US pharmaceutical clients and are looking for Senior Analysts – Managed Services to join our growing organization. This role is ideal for experienced professionals with a strong background in US pharmaceutical managed care, government pricing, and gross‑to‑net calculations, who enjoy working in a fast‑paced, client‑facing environment and want to be part of a long‑term, scalable delivery model. Key responsibilities Perform complex rebate calculations related to managed care, Medicaid, and government programs. Analyze monthly and quarterly utilization data and translate it into accurate, client‑ready deliverables. Ensure high levels of accuracy, timeliness, and SLA compliance across all assigned work. Manage recurring, production‑focused workloads with consistency and attention to detail. Support client‑facing interactions, including responding to questions and explaining analyses when required. Collaborate closely with onshore US teams and internal stakeholders. Use internal calculation tools and advanced Excel to support analysis and reporting. Required experience & skills US pharmaceutical industry experience is required. Strong background in one or more of the following areas: Managed care Medicaid Government pricing Gross‑to‑net calculations Proven experience handling complex rebate calculations. Advanced Excel skills (required). Strong analytical, problem‑solving, and critical‑thinking abilities. Clear and professional written and verbal communication skills in English. Ability to work in a fast‑paced, production‑driven environment with recurring deadlines. Nice to have Experience working for pharmaceutical manufacturers or consulting firms supporting US pharma clients. Experience with Model N or similar proprietary / competitor pricing tools. Prior client‑facing or stakeholder‑management experience. Education Bachelor’s degree preferred. Relevant industry experience may be considered in lieu of formal education. Why join us Be part of a strategic near‑shore expansion supporting US pharmaceutical clients. Join a team with long‑term growth potential and career development opportunities. Work closely with experienced global teams in a highly visible, business‑critical role. 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.

Help bring clarity, structure, and predictability to regulatory project delivery. At IQVIA, we're advancing healthcare by helping life sciences organizations navigate complex regulatory environments and bring therapies to patients faster. We're looking for a highly organized and detail-oriented Project Analyst to support the successful delivery of regulatory projects and programs across our Global Regulatory Affairs team. In this role, you'll work closely with Project Managers, delivery teams, finance partners, and stakeholders to ensure projects remain on track, risks are visible, reporting is accurate, and governance standards are consistently maintained. If you enjoy turning data into insight, coordinating across functions, and creating structure in fast-moving environments, we'd love to hear from you. What You'll DoAs a Project Analyst, you will play a key role in supporting project planning, tracking, reporting, and operational governance by: Supporting project setup, planning, and mobilization activitiesMaintaining project plans, schedules, trackers, and delivery dashboardsMonitoring milestones, action items, risks, issues, and dependenciesPartnering with project finance stakeholders to support effort tracking, forecasting, revenue reconciliation, billing activities, and scope change managementPreparing project status reports, metrics, and materials for internal and client-facing meetingsEnsuring project documentation remains complete, accurate, and audit-readyCoordinating onboarding and offboarding activities for project team membersIdentifying data inconsistencies, emerging risks, and operational issues, escalating concerns proactivelySupporting the continuous improvement and standardization of project management tools, templates, and reporting practicesRequired Skills & Experience2–5 years of experience in project support, project coordination, operational delivery, PMO, or similar environmentsStrong organizational skills and ability to manage multiple priorities simultaneouslyHigh attention to detail and commitment to data accuracyExperience maintaining project plans, trackers, reports, and documentationStrong analytical and problem-solving capabilitiesEffective communication and stakeholder coordination skillsAbility to work successfully within cross-functional and matrixed teamsProficiency with project reporting and collaboration toolsPreferredExperience within Regulatory Affairs, life sciences, healthcare, clinical research, or pharmaceutical environmentsExposure to project governance, financial tracking, forecasting, or operational reportingInterest in developing a career in project management and delivery leadershipIn this role, you'll help create: Accurate and timely project reporting that supports informed decision-makingStrong project governance and compliance with delivery processesBetter visibility of risks, issues, and project performanceReduced administrative burden for Project Managers and technical teamsImproved forecasting, financial control, and operational efficiencyConsistent, scalable delivery practices that support business growthWhy IQVIA?IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make a bigger impact on healthcare. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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

Job OverviewValidates the project scope, plans and schedules for moderately complex projects and programs; adheres to metrics for project success and begins to suggest appropriate metrics; provides input to and applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance) Essential Functions• Validates the project scope, plans and schedules for moderately complex projects and programs; adheres to metrics for project success and begins to suggest appropriate metrics; provides input to and applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance).• Facilitates Sprint Planning, Backlog Refinement, Sprint Review, Retrospectives and Daily Scrum (Stand Ups).• Supports Product Owners in short and long term release planning and  maintaining a healthy Product Backlog.• Maintains clarity and enforcement of “Definition of Done”.• Identifies risks to program success and escalates to management as necessary.• Manages project delivery process, scope, and costs of moderately complex  projects under broad supervision; drives completion of the project/program.• Manages stakeholder relationships; develops and executes communication planManages change by identifying impacts of the project, building awareness and support for change within the organization, and contributing to development of trainingEvaluates project results against success metrics; recommends or implements changes to processes, resources and solutions that improve productivity and end product. Removes impediments for team members and shields them from external interference Consistently delivers established team reporting and guidance metrics. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Requires at least 7-8 years of total experience with 2 years of Scrum Master Experience 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.