Policies and Procedures
Policies and procedures for the CRU include the following categories:
Investigator Roles and Responsibilities
- The Principal Investigator (PI) is responsible for all aspects of the study
- Contact information must be available for 24-hour access to the PI or co-investigator with clinical responsibilities for the participant.
- The PI is responsible for being familiar with the procedures of the CRU and ensuring co-investigators and coordinators are also familiar with these procedures and policies. The annotated slide set provides an overview. This presentation provides information for coordinators and investigators about undertaking a study at the CRU (policies/procedures, MD orders and scheduling).
Progress Reports, Renewal, and Revisions
Contact Us
Find out if CRC can assist you with your research efforts:
Clinical Research Centers
Tel: 212-241-6045
Hours of Operation
Monday – Friday, 7am until 7pm
Helpful Links
Institutional Review Board (IRB)
Grants and Contracts Office (GCO)
Conduits - the Institutes for Translational Sciences
Related Resources
Application [DOC]
Schedule of SAC meeting and deadlines for applications [DOC]

