The Clinical Research Coordinator (CRC) collaborates with investigators, research teams, clinical departments, IRBs, and sponsors to plan, implement, and manage clinical trials and research projects. Responsibilities include participant recruitment, screening, enrollment, conducting protocol-required visits, data collection, and coordinating sponsor monitoring or federal audits. The CRC ensures compliance with federal and state regulations, institutional policies, and maintains accurate documentation, adverse event reporting, and study drug accountability.
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Company Description We suggest you enter details here. Role Description This is a full-time, on-site Concrete Lead Carpenter role located in Salt Lake City Utah. The Lead Carpenter will be responsible for overseeing and executing carpentry projects, including ...