The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff
Job Summary
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff.
This individual obtains informed consent, collects, maintains and organizes study information.
Assists in the preparation and submission of grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office).
Matching Summary
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff.
Skills & Requirements
Must-have
Human subjects research
Informed consent process
Clinical data collection
Maintain study documentation
Microsoft Office Suite
Nice-to-have
Psychiatry research experience
Grant application assistance
Regulatory agency site visits
Key Requirements
Bachelors degree in science or related field preferred