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Assistant(e) d'Etudes Cliniques

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Primary Location: Courbevoie, France Full time R1149668

Job description

Are you passionate about working on innovative programmes in oncology, rare disease, cardiovascular, and other therapeutic areas within world-renowned top 5 pharma & biotech? Great, because we're hiring!

We're looking for innovative clinical research professionals just like you to join our global clinical operations teams across Europe, specifically in France, Rueil-Malmaison

We are hiring Clinical Trial Associates (CTA):

CTA I: Up to 2 years’ experience in global clinical trials.

CTA II: Minimum 2 years’ experience in global clinical trials. Roles that map to the CTA II category would include: Business Analyst, Finance Coordinator, Regulatory Associate

As CTA I you will be involved in the following activities but not limited to, setting up and maintaining applicable TMF (both electronic and hard copy versions). Alert management where current status of data quality or performance is at risk to noncompliance. Maintaining, updating, and inputting information and/or documents into applicable databases for clinical trial and/or data tracking; ensuring reporting system records and quality standards are appropriately maintained.

You will track incoming and outgoing clinical and regulatory documents/updates for investigator sites, studies, or project team while supporting assigned group(s) or team(s) in preparing applicable study documents. You will manage the central inbox and process site requests to appropriate team members and serve as the primary point of contact for field monitoring staff and global DRA.

As CTA II you will perform all or some of the tasks outlined under the CTA I role, and in addition, may also perform all or some of the following responsibilities:

Prepare site specific ICF and any other relevant forms according to local SOP. Prepare and compile dossier for initial HA and IRB submission or amendment and oversee associated activities, responses and communications with obtaining approvals for the assigned country(ies). Provide support for trial budget and investigator site payments; support the project manager and team with financial tasks. Maintain oversight of the entire purchase order process, from set-up to reconciliation, as well as the processing of study invoices.

IQVIA is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry dedicated to delivering unique and actionable insights. Formed through the merger of IMS Health and Quintiles, IQVIA has more than 65,000+ employees worldwide

At IQVIA, we are committed to advancing human health and delivering real value and outcomes for customers and patients. We view each day as another opportunity to find new solutions and enable the next breakthrough.

We can offer you:

•Competitive Salary Packages 

•Excellent Benefits Packages 

•Progression opportunities

•Employee Referral Scheme 

•Performance Related Bonuses 

•Expert training and guidance 

•Streamlined managerial support 

•Individualised approach to development

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at

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