Freelance Clinical Research Associate

EPM Scientific are currently partnered with a Global CRO who are seeking a Consultant Clinical Research Associate (CRA) to support their existing programmes. See a short summary below:

Contract Conditions:

• Start date: ASAP
• Location: Utrecht, Netherlands
• Contract: 0.8 FTE, 3 Month Contract
• Language: Dutch and English
• Project: Infectious Disease, Vaccine

Key Responsibilities:

• Monitor clinical trial sites in the Netherlands, 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 Dutch regulatory environment.
• Proven ability to work independently and manage multiple sites.
• Excellent communication and organizational skills.

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