Responsibilities
- Support the principal investigator in evaluating potential participants for study eligibility
- Keep accurate and up-to-date case report forms, medical charts, and research documentation
- Provide guidance, training, and supervisory support to junior coordinators and research assistants
- Ensure all clinical trial activities follow approved protocols, regulatory standards, and legal requirements
- Gather, record, and input study-related data as required
- Collaborate with leadership during recruitment efforts and onboarding of new team members
- Contribute to the initiation, ongoing management, and conclusion of research studies as needed
- Demonstrate adaptability when assigned to different research projects
