The Unblinded Clinical Research Coordinator (CRC) is responsible for coordinating all unblinded aspects of clinical trials, including investigational product (IP) management, drug accountability, and subject randomization. This role requires strict adherence to protocol while maintaining confidentiality to protect the integrity of the study.
Key Responsibilities:
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Responsible for performing quality calibration activities for the screening and donor floor area equipment. Accountable for donor center pre-registration, registration, conducting health screenings, donor center set up, and disconnects. Assist with donor center flow by...
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