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The Qualified Person Responsible for Pharmacovigilance (QPPV) is a mandatory position Marketing Authorization Holders (MAHs) are required to have when operating as entities in the European Union (EU). The QPPV is responsible for the establishment and maintenance of the MAH’s phar
The Qualified Person Responsible for Pharmacovigilance (QPPV) is a mandatory position Marketing Authorization Holders (MAHs) are required to have when operating as entities in the European Union (EU). The QPPV is responsible for the establishment and maintenance of the MAH’s phar
Job Overview Support, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating procedures (SOPs), policies and practices, good clinical practices
The Clinical Project Manager (Sponsor dedicated) will be leading Local Study Teams 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 a
- Review Requests For Proposal (RFP). Identify information for proposal text and budget development and work closely with proposal development team to prepare and finalize proposals. - Prepare text and budget for proposals, rebids and related documents. - Provide support and assi
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeuticall
To be eligible for this position, you must reside in the same country where the job is located. Please note: This hybrid position will be responsible for working in our New York, Boston, or San Francisco office 2-3 days per week. IQVIA Advisory Services is a newly established s
We are seeking Laboratory Project Services Coordinator to join IQVIA Laboratories at Buenos Aires. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we tran
Our team is growing and seeking a motivated, early-career Associate AI Engineer to help build the AI solutions that support our Health Economics and HTA Team. Working under the guidance of senior engineers, the Associate AI Engineer will contribute to turning validated prototype
Job Level: Therapeutic Strategy Director – Early Clinical Development JOB OVERVIEW Early Clinical Development is a core, complex focus at IQVIA, requiring deep expertise and integrated data-driven strategies. The Therapeutic Strategy Leader (TSL) serves as the scientific and st
We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider. IQVIA Laboratories helps sponsors
Job Overview Manage the administrative support across all Lifecycle Safety service lines to the SO and LSM functions as appropriate. Provide support to junior administrative team members. Qualifications - Education: Bachelor's degree in a life science field (e.g., biology, pha
Site Enrollment and Engagement Leads collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The role as a strategic partner to both external and internal stakeholders to optimize the site experience and perform
- Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract nego
IQVIA Biotech is seeking Sr. Site Contracts Associate or Site Contracts Associate with 3-5 years' experience negotiating clinical site contracts and budget templates. This role requires candidates who have sponsor facing experience as well. IQVIA Biotech is a full-service CRO pu
Start Date: Immediately Duration: Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Rome. This 20h hour per week role offers a unique opportunity to contribute to meaningful research in a collabo
This role is available in the UK and in the European Union. The list of countries in the job ad is not exhaustive. IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. Our Clinical Outcomes Assess
A la croisée de deux univers, la santé et les nouvelles technologies, IQVIA est l’expert des données de santé depuis plus de 60 ans et dans 140 pays. IQVIA s’appuie sur ses bases de données uniques, sur son expertise et sur ses outils d’analyse pour apporter des services et des s
Job Overview As an eCOA Implementation Project Manager, you will lead the startup phase of electronic Clinical Outcome Assessment (eCOA) projects, ensuring seamless delivery for sponsors and clinical teams. You’ll manage timelines, budgets, and stakeholder communications while d
Job Overview Develop fit for purpose applications, backend services, integrations, and platform capabilities to support digital measurement, healthcare, and AI/ML-enabled products. Design, build, test, deploy, and maintain production-grade applications, APIs, backend services, d
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