Site Management Associate I

Exchange data, documents, and project-relevant information between investigative sites, vendors, and the project team while serving as the main site contact for administrative and non-protocol matters. Prepare regulatory and ethics committee submission documents, coordinate site payments and trial supplies, and support query resolution and EDC completion tracking. Organize internal meetings and investigator meetings, coordinate trial-related training, and maintain Trial Master File and Investigator Site File records. Track site issues in CTMS and ensure proper safety information flow with investigative sites. Provide miscellaneous administrative support and facilitate communication between all stakeholders. Maintain hybrid work in Ankara.