Clinical Research Associate II
Hybrid · São Paulo, São Paulo, Brazil
Job Summary
Clinical Research Associate II responsible for monitoring activities at clinical sites, ensuring adherence to GCP/ICH guidelines and AbbVie SOPs, overseeing start-up, execution, and close-out of studies across Phase 1-4, coordinating site qualification/initiation/interim monitoring visits, ensuring data quality and timely reporting of safety events, maintaining regulatory inspection readiness, training site personnel on protocol requirements, and managing investigator payments and site agreements.
Required Qualifications
- Minimum of 1 year of clinically-related experience, of which a period of 6 months is preferable in clinical research monitoring
- Experience in on-site monitoring of investigational drug or device trials is required
- Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred
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