Senior Clinical Research Associate

Job Summary

Working remotely as a freelance Senior Clinical Research Associate, the candidate will manage the initiation, monitoring, and closeout of clinical study sites, ensuring compliance with regulatory requirements and company policies.

Key Responsibilities:

• Monitor clinical trials on-site and remotely, ensuring subject safety, data integrity, and compliance with GCP and ICH guidelines
• Verify informed consent procedures and protocol compliance to protect study participants
• Prepare monitoring visit reports, document findings, and maintain study documentation in accordance with regulatory requirements

Required Qualifications:

• Bachelor's Degree in Life Sciences, Nursing, or equivalent
• More than 3 years of experience as a Clinical Research Associate with significant on-site monitoring experience
• Strong understanding of Good Clinical Practice (GCP) and ICH guidelines
• Experience managing clinical sites through all phases of clinical trials
• Fluency in English with strong organizational abilities