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?

Write a protocol

If you would like to write a protocol, start with one of these templates.

GW Cancer Center Protocol Template Phase 2

GW Cancer Center Observational Study Protocol Template

Submit a protocol for review

What do I need to submit?

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.

Get coordinator help for a study

Coordinators can assist with study needs, depending on availability. To learn more or request assistance, please contact Dr. Richard Lush at rmlush3@gwu.edu.

Access OnCore and/or EDC and find training materials

Visit the Accounts and Support page to request a user account, log in and access training materials.

Find additional trainings

A variety of trainings and resources are available through the CTSI-CN website.

Navigation Assistance

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

800 22nd Street NW, Suite 8390
Washington, DC 20052
(202) 994-0872 or email PRMS@gwu.edu