Location
sao paulo, sao paulo, Brazil
Posted
July 18, 2026
Job Description
**Responsibilities include, but are not limited to**:
- The role is accountable for performance and compliance for assigned protocols and sites in a country;
- Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally;
- Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites;
- Actively develops and expands the territory for clinical research, finding and developing new sites;
- Participates in internal meetings and workstreams as SME for monitoring processes and systems;
- Develops strong site relationships and ensures continuity of site relationships through all phases of the trial;
- Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, L...
- The role is accountable for performance and compliance for assigned protocols and sites in a country;
- Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally;
- Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites;
- Actively develops and expands the territory for clinical research, finding and developing new sites;
- Participates in internal meetings and workstreams as SME for monitoring processes and systems;
- Develops strong site relationships and ensures continuity of site relationships through all phases of the trial;
- Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, L...