Clinical Research Associate
1 month ago
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 manage clinical trial sites, conduct on-site visits, and collaborate with the project team to ensure the success of the study.
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.
Meet the Requirements:
- 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.
What We Offer:
- Full-time freelance engagement.
- Remote work opportunity.
- Opportunity to work on oncology clinical trials.
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