Freelance Clinical Research Associate

EPM Scientific are currently partnered with a pioneering biopharmaceutical company dedicated to advancing treatments for rare neurological disorders. They are urgently seeking a Consultant Clinical Research Associate (CRA) to support a high-priority clinical program in rare neurological disease. See a short summary below: Contract Conditions: Start date: August, FlexibleLocation: France (Remote flexibility with occasional site visits)Contract: 0. 5 FTE, Possibility to Increase over timeLanguage: French and English requiredProject: Rare Neurological DiseaseKey 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: Minimum 5 years of experience as a CRA, ideally with exposure to rare disease or neurology trials. 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.

Experience with eTMF and EDC systems is a plus. If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.