Clinical Research Associate
il y a 3 semaines
Job Title: Freelance Clinical Research Associate (CRA)
Location: Remote
Job Type: Freelance Full-Time
Job Description:
Meet is seeking an experienced Freelance Clinical Research Associate (CRA) to manage oncology-focused clinical trials. The ideal candidate is passionate about advancing medical knowledge and excels in a fast-paced, detail-oriented work environment.
Key Responsibilities:
- Clinical Site Management: Oversee clinical trial sites to ensure compliance with study protocols, timelines, and regulatory guidelines.
- Monitoring and Auditing: Conduct on-site visits, routine monitoring, and audits for clinical trials, focusing on oncology and immunology studies.
- Data Management: Collect, review, and manage trial data, ensuring accuracy, completeness, and timely submission.
- Collaboration: Work closely with the project team, acting as a key point of contact for investigators and site staff, to ensure the smooth operation of clinical trials.
- Regulatory Compliance: Ensure adherence to Good Clinical Practice (GCP) and other regulatory requirements throughout the study lifecycle.
- Reporting: Provide detailed reports on study progress, including site performance, data collection, and any deviations from protocols.
Qualifications:
- 3+ years of experience as a Clinical Research Associate (CRA), with a proven track record in immunology trials.
- Strong understanding of ICH-GCP guidelines and regulatory requirements.
- Experience managing clinical trials, from site initiation to closeout.
- Immunology therapeutic area experience is highly desirable.
- Exceptional communication and interpersonal skills to collaborate with project teams and site staff effectively.
- Ability to manage multiple sites and projects independently.
- Fluency in French is required; proficiency in English is a plus.
- Highly organized with a strong attention to detail.
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