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

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