Freelance Clinical Study Co-ordinator

il y a 2 semaines

Paris, France EPM Scientific Temps plein

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_
- _ 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 logístical 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._

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