As a Clinical Research Associate, you’ll be fully dedicated to one of our global pharmaceutical partners — a collaboration founded on shared values of innovation, flexibility, and a united mission to bring life-changing treatments to patients more quickly.

This is your chance to join an exclusive, high-impact program where you can lead by example and help set the benchmark for clinical excellence.

Location: Paris-based position, with 2-3 days per week at the sponsor’s office in Puteaux or on-site visits, and 2 days working from home.
Profile: We’re seeking experienced CRO CRAs with at least 3 years of independent monitoring experience.

Key responsibilities include: 

• Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
• Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

You will need:

• A solid, stable background as a CRA with at least 3 years of experience

• An interest in working across diverse therapeutic areas, including diabetes, cardiology, rare diseases, and obesity (Phase 2-3 studies)

• Excellent organizational skills

• The ability to thrive in a dynamic environment, prioritize effectively, and adapt to changing business needs

• Strong IT skills

• Outstanding communication skills, with the capacity to multitask and perform well under pressure

• Fluency in French and professional proficiency in English

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