- Remote, Peru
- Remote
- Senior
- 3–5 years
Senior Clinical Research Associate responsible for monitoring clinical studies, ensuring compliance with ICH-GCP and company SOPs, and managing site visits and data quality.
Responsibilities
- Conducts independent monitoring visits and remote data checks
- Prepares and finalises monitoring visit reports in CTMS
- Manages study supplies and drug accountability
- Ensures compliance with regulatory requirements and company policies
- Collaborates with local MSLs and study teams