Clinical Trial Manager (CTM)

■Responsibilities
・Effective Management of a project including:
Coordinate and manage project start-up, project maintenance, and project close-out activities;
Maintain ongoing Sponsor contact for project-specific issues by serving as primary contact for Sponsor and all project team members;
Track study status including patient status, Case Report Form status, safety issues, timelines, etc.;
Serve as primary contact for protocol interpretations and logistical project-related issues (internal and external);

・Provide management oversight for Clinical Research Associates and Project Coordinators on project team;
Interpret contract-related issues and coordinate Medpace activities according to current scope;
Develop study management tools, including communication plan, clinical monitoring plan, patient recruitment and retention plan;
Communicate change in scope to Sponsor clinical team and Medpace Contract Manager.
Provide input for following (when applicable):
Study protocol
Edit Check Specifications
Data Analysis Plan
Data clean-up results
Analysis
Final study report