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Job Description
📋 Description Independently conduct onsite and remote site monitoring and close-out visits in accordance with Collaborate with site staff to ensure data consistency with source documents and study requirements. Monitor and resolve data queries; escalate issues as appropriate. Coordinate shipment of clinical supplies (investigational product, lab supplies, ePROs, study Ensure site staff are trained on protocol, study plans, systems and ICH-GCP. Participate in routine study progress meetings and Investigator’s meetings. 🎯 Requirements College diploma/degree with 4-6 years of related experience. Regular travel to sites; up to 40-60% depending on project and location. Proficient in EDC systems (Medidata Rave, Oracle InForm), IRT, eTMF, CTMS, and Microsoft Office Strong interpersonal, problem-solving, organization, and communication skills; ability to work
