Responsibilities
- Support the principal investigator in evaluating and confirming eligibility of potential study participants
- Manage and update case report forms, medical charts, and related 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 required study data accurately and in a timely manner
- Collaborate with leadership during recruitment efforts, including candidate evaluation and onboarding shadowing
- Support initiation, ongoing management, and conclusion of research studies as assigned
- Demonstrate adaptability when reassigned to different studies based on team needs
