Freelance Clinical Study Co-ordinator

EPM is working with a leading CRO seeking a freelance Clinical Study Coordinator for an exciting project. This is a unique opportunity to contribute to cutting-edge genomic research in precision medicine. See a short summary below:

Contract Conditions:

• Start date: ASAP
• Location: France, EU Remote Considered for strong candidates
• Contract: 6-month, Potential to extend
• Language: English (additional European languages are a plus).

Key Responsibilities:

• Guarantee the integrity, completeness, and high quality of clinical data gathered from study sites.
• Oversee the organization and maintenance of essential documentation, including Trial Master Files (TMF) and Investigator Site Files (ISF).
• Manage logistical aspects of the study, such as coordinating the delivery of materials, handling documentation, and overseeing shipment processes.
• Provide operational support across various functions, including financial tracking, translation coordination, and progress reporting.
• Contribute to the planning and execution of key clinical trial meetings, including investigator and internal team sessions.

Requirements:

• Strong (5 years preferred) experience in clinical research (CRO, biotech, pharma, or clinical research unit).
• Experience in oncology essential
• Willingness to travel as required.
• Fluency in French and English is essential.

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