Freelance Clinical Research Associate

il y a 1 jour

Paris, France EPM Scientific Temps plein

EPM Scientific are currently partnered Global CRO who are seeking a Consultant Clinical Research Associate (CRA) to support a muhltiple programmes. See a short summary below:
**Contract Conditions**:

- _ Start date: ASAP_
- _ Location: France (Remote)_
- _ Contract: 0.8-1 FTE, 6-12 Month Contract_
- _ Language: French and English required_
- _ Project: Oncology, Hematology, Neurology_

**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**:

- _ Strong (5+ years preferred) experience as a CRA._
- _ 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._

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