Freelance Clinical Research Associate

EPM Scientific; Paris; À distance; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A global CRO is seeking a Consultant Clinical Research Associate (CRA) to monitor clinical trial sites in France. This role involves ensuring compliance with regulations, maintaining documentation, and collaborating with cross-functional teams. The ideal candidate has at least 5 years of CRA experience and is fluent in French and English. This position supports a mix of oncology, hematology, and neurology projects. Competitive remote work options are offered.

Qualifications

• Minimum 5 years of experience as a CRA (preferred).
• Proven ability to work independently and manage multiple sites.

Responsabilités

• Monitor clinical trial sites across France for compliance.
• Act as the primary contact for site staff on various activities.
• Ensure accurate documentation and reporting aligned with timelines.
• Collaborate with cross-functional teams including project managers.
• Contribute to risk-based monitoring strategies and audits.

Connaissances

Strong knowledge of ICH-GCP

Fluency in French

Fluency in English

Excellent communication skills

Excellent organizational skills

Description du poste

EPM Scientific is currently partnered with a global CRO seeking a Consultant Clinical Research Associate (CRA) to support multiple programmes. Below is a brief overview:

Contract Details:

• Start date: ASAP
• Location: France (Remote)
• Contract: 0.8-1 FTE, 6-12 months
• Languages: French and English required
• Projects: Oncology, Hematology, Neurology

Key Responsibilities:

• Monitor clinical trial sites across France, ensuring compliance with GCP, protocol, and regulatory requirements.
• Act as the primary contact for site staff, supporting site initiation, monitoring, and close-out activities.
• Ensure accurate documentation, data collection, and reporting aligned 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 (preferred)
• Strong knowledge of ICH-GCP and the French regulatory environment
• Proven ability to work independently and manage multiple sites
• Excellent communication and organizational skills
• Fluency in French and English is essential

If interested, please apply directly to learn more. Feel free to share this opportunity within your network.