Snabbfakta
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- London
Ansök senast: 2024-12-31
Freelance clinical research associate
Publicerad 2024-11-01
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.
