Clinical Research Assistant
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About The Position
The Clinical Research Assistant works under direct supervision and assists research coordinators with organizing, gathering, and compiling clinical research data. This role involves tracking and maintaining credentialing documentation for staff and all researchers participating in clinical trials in accordance with IRB regulations. The assistant may provide clerical and technical support to ensure adherence to research protocols and the quality of information received. Responsibilities include performing a variety of research, database, and clerical duties in support of clinical trials to assist investigators in organizing, gathering, and compiling clinical research data. The assistant is responsible for organizing and maintaining documentation required for clinical trial(s) and informing the Principal Investigator and/or designated individual on any issues concerning patient responses to treatment, medication, or any adverse effects overall to patients. Additionally, the assistant may assist the Principal Investigator with IRB filings and annual reviews and may help in the enrollment of human subjects.
