ProPharma is seeking an experienced Clinical Research Associate to support monitoring in Italy. The role involves clinical monitoring, data review, and query resolution for assigned protocols and investigational sites.
Requirements
- Bachelor's degree or equivalent combination of education and experience
- 2+ years of experience as a Clinical Research Associate
- Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials
- Electronic data capture (EDC) experience required and CTMS and IVRS system experience is a plus
- Rare disease or Pediatric experience would be preferred
Benefits
- Initial 1 year contract at 0.1 - 0.2 FTE
- Opportunity to work on a hybrid basis with in-person collaboration encouraged
