Clinical Research Associate

Job Summary

To support clinical trials, the part-time freelance Clinical Research Associate will monitor study sites both on-site and remotely, ensuring compliance with regulatory requirements and maintaining data integrity in a fully remote capacity.

Key Responsibilities:

• Monitor clinical trials in accordance with company policies, GCP, ICH guidelines, and regulatory requirements to ensure subject safety and data quality
• Verify informed consent procedures and protocol compliance, ensuring the protection of study participants
• Prepare monitoring visit reports, document findings, and update project systems with accurate site information

Required Qualifications:

• Bachelor's Degree in Life Sciences, Nursing, or equivalent
• Minimum 1 year of relevant clinical research experience or academic background related to clinical trials
• Understanding of Good Clinical Practice (GCP) and ICH guidelines
• Strong written and verbal communication skills in English
• Excellent organizational skills and ability to work independently in a matrix team environment