The overall objective of this position is to obtain informed consent to participate in research studies, including a COVID-19 surveillance study. Reporting to the Principal Investigator, the Clinical Research Coordinator will obtain informed consent, coordinate self-collection of biospecimens (i.e., saliva, nasal swab), and administer study questionnaires to be used for future research purposes. New patients will be approached through a combination of remote recruitment through REDCap and in-person recruitment through outpatient clinics. The coordinator will serve as the primary contact for research participants, study sponsors, Principal/ co-investigators, and other study staff.
The CRC will work with investigators, study staff, the CUIMC institutional review board (IRB), research study sponsors and federal regulatory agencies to assure compliance with study protocols, data documentation, and reporting requirements. The incumbent will perform other related duties as assigned.
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