The Office of Clinical Research serves as a resource on clinical trials and study management for both Wake Forest Baptist Health and the local community. The Office of Clinical Research's centralized administration focuses on protocol implementation, study coordination, data and regulatory management, clinical trial budget development, internal auditing and clinical trial education.
- Work with study teams to implement quality clinical trials that are activated quickly.
- Assist in identification and allocation of resources for conducting clinical trials.
- Assess trial accrual potential and plausible overlap between competing trials.
- Create an infrastructure to support and promote appropriate research billing.
- Maintain a current registry of all consented clinical research participants.
- Develop tools, resources, and training for the clinical research community.
Clinical Trials Facilitation
The Office of Clinical Trials provides expertise to investigators on protocol development, navigating the IRB system and addressing other regulatory concerns and issues as part of the clinical trial process.
Contact: Selvin Ohene | email@example.com | 336-716-9134