Freelance Clinical Research Associate (CRA) – Job Description

We are looking for an experienced Freelance Clinical Research Associate (CRA) to support ongoing and upcoming clinical trials. The ideal candidate will be responsible for monitoring clinical sites, ensuring compliance with Good Clinical Practice (GCP), and facilitating communication between stakeholders.

Key Responsibilities:

• Oversee site selection, initiation, monitoring, and close-out visits.
• Ensure compliance with GCP, protocols, and regulatory requirements.
• Collaborate with investigators and site staff to ensure accurate data collection.
• Identify and resolve protocol deviations and data discrepancies.
• Provide timely updates and reports on trial progress.

Requirements:

• Proven experience as a Clinical Research Associate (CRA)
• Strong knowledge of GCP, ICH guidelines, and local regulatory requirements.
• Experience in on-site and remote monitoring.
• Fluency in English Finish and/or Danish
• Availability for 0,6FTE for Denmark and 0,4FTE for Finland

👉 This role can be split between two freelancers depending on language skills and availability.