Senior Clinical Trials Assistant

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

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 the world, specifically in France

We are hiring Senior Clinical Trial Associate (SrCTA) with 8-10 years’ experience in global clinical trials.

As SCTA 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.

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.

Ensure the successful negotiation and ongoing management of clinical trial agreements with investigative sites and vendor agreements and associated budget management. Maintain accurate records, metrics and reports; identify gaps and report to management; make recommendations for process improvement and efficiencies

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.