Freelance Clinical Research Associate

EPM Scientific are currently partnered Global CRO who are seeking a Consultant Clinical Research Associate (CRA) to support a muhltiple programmes. See a short summary below:

Contract Conditions:

• Start date: ASAP
• Location: France (Remote)
• Contract: 0.8-1 FTE, 6-12 Month Contract
• Language: French and English required
• Project: Oncology, Hematology, Neurology

Key Responsibilities:

• Monitor clinical trial sites across France, ensuring compliance with GCP, protocol, and regulatory requirements.
• Serve as the primary point of contact for site staff, supporting site initiation, monitoring, and close-out activities.
• Ensure timely and accurate documentation, data collection, and reporting in line with project timelines.
• Collaborate with cross-functional teams including Clinical Project Managers, Medical Monitors, and Regulatory Affairs.
• Contribute to risk-based monitoring strategies and support audit readiness.

Requirements:

• Strong (5+ years preferred) experience as a CRA.
• Strong knowledge of ICH-GCP and French regulatory environment.
• Proven ability to work independently and manage multiple sites.
• Excellent communication and organizational skills.
• Fluency in French and English is essential.

If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.