Clinical Research Associate
Job Summary
To support clinical trial initiatives, the freelance Clinical Research Associate (0.4 FTE) will conduct remote and on-site monitoring, ensuring compliance with regulatory requirements and data integrity while working fully remotely.
Key Responsibilities:
- Monitor clinical trials to ensure subject safety, data integrity, and compliance with GCP and ICH guidelines
- Verify informed consent procedures and protocol adherence at study sites
- Prepare monitoring visit reports and maintain accurate site documentation in project systems
Required Qualifications:
- Bachelor's Degree in Life Sciences, Nursing, or a related field
- Minimum 1 year of relevant clinical research experience or academic background in clinical trials
- Understanding of Good Clinical Practice (GCP) and ICH guidelines
- Fluency in English with strong written and verbal communication skills
- Excellent organizational skills and ability to work independently in a matrix team environment
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