Clinical Trials Management Office
Definitions – Investigator Initiated Clinical Trials Workflow
OSP:
Please contact the Office of Sponsored Programs as soon as you begin to consider submitting a grant proposal. Developing a successful application requires significant time and preparation. The office is here to help ease the administrative burden and reduce errors that may potentially remove your proposal from consideration by a sponsor.
Principal Investigators (PI) should complete the Notification of Intent to Submit form no later than 10 business days before the sponsor deadline. Early notification is strongly recommended. Before notification can occur, the PI should reach out to the appropriate Academic Vice Chair to discuss the proposed project and potential ramifications for GHS.
To assist you with the process, we have compiled information necessary to complete your grant proposal. Visit our Grant Proposal Information page for institutional information as well as administrative and fiscal contacts for GHS.
Additionally, you may access other materials necessary for submitting a grant proposal by visiting our Forms & Policies page.
Contact Information:
Hagan Walker, MS, MBA
Manager, Office of Sponsored Programs
864-455-9861
Clinical Trials Management Office
The Clinical Trials Management Office provides comprehensive support forclinical trialsresearch. The office serves as a central resource forGHSresearchers, staff and departmentsinvolved in clinical trials research and for sponsors seeking to conduct clinical trials atGHS by:
· Serving as an expert resource for information on the issues and requirements for the conduct of clinical research
· Developing and providing education on the requirements and procedures related to the conduct of clinical research
· Serving as the primary point of contact for questions or issues related to clinical trials
· Assisting GHS researchers, staff and departments with clinical trial project development
· Provide assistance and consultation in budget development and preparation
· Interacting and communicating with sponsors, CROs and other entities on behalf of the institution, researchers and departments on issues related to clinical trials
· Developing and implementing programs and initiatives, based on monitoring and assessment, to enhance the quality of clinical research and support regulatory compliance
· Providing oversight and assisting with registration of clinical trial information and posting of results as appropriate
For more information, contact the CTMO ()