Clinical Research Associate

Role: Clinical Research Associate responsible for site management and monitoring of investigator sites in clinical trials to ensure patient safety, GCP compliance, and study quality. Main objectives include site oversight from initiation through close-out, facilitating trial activities, and maintaining site engagement. Responsibilities encompass managing site conduct per protocols, supporting recruitment, conducting remote and onsite monitoring, addressing protocol deviations, AE/SAE reporting, and ensuring proper investigational product oversight. Qualifications: Bachelor's in life sciences or related field; minimum 1 year clinical research site monitoring experience; knowledge of GCP, ICH, FDA regulations; preferred oncology, vaccines, or infectious disease experience; fluency in English and local language. High-value biopharma specifics: involvement in global trials, focus on patient safety, regulatory compliance, and protocol adherence. Cross-functional collaboration with study teams and Site Care Partners required. Work setup involves significant travel (60-80%), including international travel, with a valid driver’s license and passport.