Role OverviewA Clinical Research Coordinator 1 (CRC 1) is a research professional who works under the guidance and supervision of their leader, responsible for managing all the day-to-day activities of clinical trials.
What You Will Do
The CRC 1 prepares study specific source documents, continuously monitors the safety and rights of the participants, documents all required data in the sponsor's data capture tool, and reports all adverse and serious adverse events.
Why It Might Be a Fit
The CRC 1 works closely with the sponsor representatives and the Principal Investigator, as well as the ancillary departments within the Office of Clinical Research.
Requirements
- Bachelor's Degree in Science, Business Administration, or Health-related field
- One to two years of experience as a Clinical Research Coordinator/Associate managing a portfolio of clinical research studies and their participants
- One year of relevant patient-facing clinical experience (such as Nurse Aid, Patient Care Technician (PCT), Medical Assistant (MA), Phlebotomist)
- Training in Phlebotomy within 3 months of hire, if no prior Phlebotomy experience
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