Freelance Clinical Research Associate


Paris
Contract
Negotiable
Clinical Development
CR/552595_1753266192
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, Flexible
  • Location: France (Remote flexibility with occasional site visits)
  • Contract: 0.5 FTE, Possibility to Increase over time
  • Language: French and English required
  • Project: Rare Neurological Disease


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:

  • 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.

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