Senior Clinical Research Associate

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