Freelance clinical research associate

Job Title: Freelance Clinical Research Associate (CRA) – Full-Time

Location: Remote/Europe

Job Type: Full-Time Freelance (FTE 1.0)

Job Description:

We are seeking an experienced Freelance Clinical Research Associate (CRA) to join our team for full-time engagement. This position requires extensive experience in oncology clinical trials, strong project management skills, and a passion for advancing medical research. If you are detail-oriented, have a deep understanding of oncology protocols, and excel in a dynamic, fast-paced environment, we want to hear from you!

Key Responsibilities:

• Monitor and manage clinical trial sites to ensure compliance with protocols, regulatory guidelines, and study timelines.
• Conduct on-site visits, monitoring, and audits for oncology-focused trials.
• Collaborate closely with the project team to ensure the success of the study.
• Collect, review, and manage clinical trial data to ensure accuracy and completeness.
• Ensure adherence to Good Clinical Practice (GCP) and other regulatory requirements.
• Provide regular updates and detailed reports on study progress.
• Act as the point of contact for investigators and clinical site staff.

Qualifications:

• 3+ years of experience as a Clinical Research Associate (CRA).
• Oncology therapeutic area experience is required.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Experience in monitoring clinical trials, from site initiation to closeout.
• Excellent communication and interpersonal skills.
• Ability to work independently and manage multiple clinical sites.
• Strong attention to detail and organizational skills.