The Clinical Research Coordinator III will oversee and coordinate complex clinical research studies, serve as a resource to provide comprehensive information to clinical research staff, promote smooth clinical operations, prepare regulatory compliance documents, coordinate interaction with other departments, and supervise clinical research coordinators and staff.
Requirements
- Acts as the primary liaison to PI in developing plans for clinical research projects
- Collaborates in the preparation of manuscripts for publication and preparation of grant proposals to sponsoring agencies
- Evaluates and interprets collected clinical data in conjunction with PI as appropriate
- Manages protocol study start up and study launch, submission, and maintenance of essential regulatory documents
- Responsible for the development of forms, questionnaires and the application of research techniques
- Provides guidance and supervision to members of research team in the implementation and evaluation of clinical research
- Performs other duties incidental to the work described above
Benefits
- Up to 22 days of vacation
- 10 recognized holidays
- Sick time
- Competitive health insurance packages
- Metro transit U-Pass
- Defined contribution (403(b)) Retirement Savings Plan
- Wellness challenges
- Annual health screenings
- Mental health resources
- Mindfulness programs and courses
- Employee assistance program (EAP)
- Financial resources
- Access to dietitians
- Caregiver leave
- Family care resources
- Tuition coverage