Welcome to the Clinical Trials Office
The objective of this office is to facilitate the process of moving clinical trials from initial proposal to successful completion in a regulatory-compliant fashion. This includes review and execution of confidentiality disclosure agreements, cost and feasibility analysis, budget development and contract execution. In addition, this office also provides financial oversight and invoicing for clinical trials.
What would you like to do?
If you would like to write a protocol, start with one of these templates.
What do I need to submit?
- Completed Protocol Review and Monitoring Committee (PRMC) Submission Form along with the protocol
- If your study involves an investigational drug, please submit your Investigator's Brochure or other details about the drug(s) involved
When do I need to submit the form?
The Protocol Review and Monitoring Committee (PRMC) meets on the first Thursday of each month. To be considered for review, the completed form, protocol and Investigator's Brochure (if relevant) must be submitted at least two weeks prior to the meeting date.
Coordinators can assist with study needs, depending on availability. To learn more or request assistance, please contact Dr. Richard Lush at email@example.com.
Visit the Accounts and Support page to request a user account, log in and access training materials.
Visit the Clinical and Translational Science Institute at Children's National (CTSI-CN) website to learn more and access REDCap.
Need help planning or conducting a clinical study? Our staff can evaluate your needs, guide you through the various stages of carrying out a clinical study and connect you with many resources available across the George Washington University (GW) and the GW Cancer Center.
CLINICAL TRIALS OFFICE