We are seeking motivated, reliable, and dedicated Clinical Research Associates (CRAs) with at least 1 year of experience as a CRA within a CRO. Ideally, you should have experience in Oncology and Onco-Hematology, although other therapeutic areas will also be considered, especially if gained in Phase I - III commercial trials.

As a Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients, where we share a culture of innovation, flexibility, and a common vision to bring life-saving treatments to market. You will set the standard for excellence and enjoy a challenging and rewarding career within our exclusive programs.

We are currently looking for a CRA based in the Paris area, who is willing to travel to the Sponsor's office for study meetings and team meetings (around once a month).

Key Responsibilities:

• Take full ownership of investigator sites for assigned studies, managing the site from start to close-out.
• Plan and conduct site visits (feasibility, site selection, interim, and close-out) in accordance with the clinical monitoring plan.
• Build strong relationships with investigator site staff to ensure key clinical metrics are met.
• Prepare for and attend investigator meetings, coordinate the timely shipment and proper storage of clinical supplies, and follow-up on drug safety issues.
• Ensure the integrity of clinical data, maintaining site tracking records and adhering to relevant guidelines.