CRA I

This role serves as the primary point of contact for clinical trial sites, overseeing the entire lifecycle from feasibility assessment and qualification to routine monitoring and study closure. Responsibilities include coordinating regulatory submissions, executing Clinical Trial Agreements, managing site initiation visits, and ensuring strict adherence to ICH GCP standards and data integrity protocols. The incumbent utilizes risk-based monitoring approaches to support enrollment goals, maintain ethical integrity, and facilitate effective collaboration between BMS and external partners.