Clinical Research Associate I/ Clinical Research Associate II

📋 Description

• Monitor and own progress of clinical studies at investigative sites.
• Ensure studies are conducted, recorded, and reported per protocol and ICH-GCP.
• Coordinate setup and monitoring: identify investigators, regulatory submissions.
• Remote role in France with travel to sites; based in Paris area.
• Smaller CRO with influence and direct-line management support.

🎯 Requirements

• Life science degree or equivalent experience.
• 1+ year as a CRA in CRO or pharma; site management experience.
• Experience managing oncology studies.
• Domestic travel with overnight stays; international travel may be required.
• Excellent communication and organizational skills; team player.
• Fluency in English and local language of country where based.
• Study start-up activities experience (preferred).

🎁 Benefits

• Strong CRA retention and good work-life balance.
• Support from direct line management and opportunities to influence.
• Remote-based role with travel to sites.