Clinical Trial Coordinator
Duke Clinical Research Institute, Clinical Operations Group
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Amber S. Brock is a Clinical Trial Coordinator (CTC) with over 12 years of experience in clinical trials. As a CTC in the Clinical Operations Group (COG) at the Duke Clinical Research Institute (DCRI), Amber onboards and trains new team members to their respective Site Management and Monitoring (SM&M) role. She also provides focused SOP training on Essential Regulatory Documents and Informed Consent Document (ICD) review while providing guidance and support to clinical study teams. Amber is part of an internal COG CTC Working Group, which focuses on creating efficiencies to streamline working practices across roles, and has also assisted in creating administrative guidelines and feedback and revisions to SOPs. Prior to working for the DCRI, she worked as a research Study Coordinator with Duke Nicotine Research through Duke University’s Department of Psychiatry and at two different Contract Research Organization as a Start Up Specialist where she honed her skills with clinical site activation for enrollment and negotiation of site specific informed consents, contracts, and budgets. Amber earned a bachelor’s degree in Psychology at Meredith College, where she received a research stipend to complete undergraduate research. Her research findings were presented at two different undergraduate research conferences: Meredith College Celebrating Study Achievement through the Meredith College Undergraduate Research Program and the Annual Carolinas Psychology Conference hosted jointly by Meredith College and N.C. State, one of the longest running undergraduate psychology conferences in the nation.
Expertise: Essential Regulatory Documents training, Informed Consent Document Review Training and proper documentation of review
Ask about: Regulatory documentation and elements of informed consent in accordance with the Code of Federal Regulations (CFR) and International Conference on Harmonization and Good Clinical Practice (ICH/GCP)
