- Sao Paulo, Sao Paulo, Brazil
Support and manage clinical trial sites throughout all phases of the study lifecycle, ensuring compliance, data quality, and patient safety.
Responsibilities
- Serve as the primary contact for assigned research sites throughout the clinical study lifecycle.
- Build and maintain strong relationships with investigators and site staff.
- Conduct remote and on-site monitoring activities in compliance with ICH-GCP, local regulations, protocols, and company procedures.
- Perform site visits, including site qualification, initiation, monitoring, and close-out visits.
- Review and maintain study and regulatory documentation throughout study start-up, maintenance, and close-out.
Requirements
- Bachelor's degree in Life Sciences
- Bachelor's degree in Pharmacy
- Bachelor's degree in Nursing
- Bachelor's degree in Biology
- Bachelor's degree in Biomedicine
