Freelance Clinical Study Co-ordinator

EPM Scientific; Paris; Hybride; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading clinical research organization is seeking a freelance Clinical Study Coordinator in Paris to manage clinical trials and ensure data integrity. The ideal candidate will have strong experience in clinical research, especially in oncology, and be fluent in both French and English. This 6-month contract offers the potential for extension, with remote work considered for strong candidates.

Qualifications

• Strong experience (5 years preferred) in clinical research.
• Experience in oncology is essential.
• Willingness to travel as required.
• Fluency in both French and English.

Responsabilités

• Guarantee the integrity, completeness, and high quality of clinical data.
• Oversee organization and maintenance of essential documentation.
• Manage logistical aspects of the study.
• Provide operational support across various functions.
• Contribute to planning and execution of key clinical trial meetings.

Connaissances

Clinical research experience

Oncology expertise

Fluency in French

Fluency in English

Description du poste

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.

Contract Conditions :

• Start date : ASAP
• Location : France, EU (Remote considered for strong candidates)
• Contract : 6-month, with 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 experience (5 years preferred) in clinical research (CRO, biotech, pharma, or clinical research unit).
• Experience in oncology is essential.
• Willingness to travel as required.
• Fluency in French and English is essential.

If this role interests you, please apply directly with your English CV. Feel free to share this opportunity within your network.