Responsibilities
- Support the principal investigator in evaluating potential participants for study eligibility
- Manage and update case report forms, medical charts, and related documentation
- Provide guidance, training, and supervisory oversight to junior coordinators and research assistants
- Ensure all clinical research activities follow approved protocols and adhere to regulatory standards and legal requirements
- Gather, record, and input data as required by the study
- Collaborate with leadership during recruitment and onboarding of new team members, including shadowing processes
- Contribute to initiating, managing, and closing research studies as needed for team projects
- Demonstrate adaptability when assigned to different studies or shifting priorities
