The Research Coordinator for Personalized Medicine will be responsible for providing clinical care services, including consenting, treating, and monitoring patients. The role involves recruiting and screening candidates for clinical trials, acquiring past medical and medication history profiles, shipping lab samples, and dispensing research drugs to patients according to protocol. The coordinator will utilize electronic capture to update patient information and help oversee clinical data for audits and oversight visits. Additionally, the position requires performing a variety of research, data entry, and regulatory duties related to departmental research endeavors, ensuring adherence to protocols and quality of information received. The coordinator will identify and screen study participants, enroll subjects in trials, assist with budget proposals and study budget tracking, ensure compliance with regulations for the protection of human subjects, complete regulatory submissions for the Institutional Review Board (IRB), and communicate with physicians and other departmental personnel as required for study design and implementation. The role also includes completing data abstraction and timely reporting of study-related adverse events to the sponsor.
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Job Type
Full-time
Career Level
Entry Level
Education Level
Bachelor's degree