Clinical Research

• Acting as a liaison between the Principal Investigator (PI), Institutional Review Board (IRB), other hospital departments, and study participants for study management.
• Provides study information to physicians, nurses, pharmacists, and lab personnel.
• Arranges in-service trainings as appropriate.
• Responsible for implementation, data management, and follow up of clinical trials to ensure data accuracy, study participant safety, confidentiality, protocol compliance, and regulatory compliance as required by the clinical trial protocol and the study sponsor.

Clinical Research Coordinator I – Non RN

Principal Clinical Scientist

Senior Principal Scientist, Clinical Research, HIV

Principal Scientist, Clinical Research, Immunology

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