Role OverviewThe Clinical Research Coordinator will work with the Principal Investigator (PI) to develop study recruitment strategies, screen referred candidates, and guide patients through informed consent. The coordinator will also serve as the principal liaison between the study agency, investigators, regulatory agencies, and study participants.
What You Will Do
The main day-to-day responsibilities of the Clinical Research Coordinator will include coordinating patient visits, follow-ups, and lab visits, recording and reviewing patient and study data, preparing and submitting documents to the IRB, and reporting adverse events.
Why It Might Be a Fit
To be a good fit for this role, you should have strong organizational skills, be able to work independently, and have excellent communication skills. You should also be able to work in a fast-paced environment and be able to adapt to changing priorities.
Requirements
- High School diploma or GED
- Ability to work independently
- Excellent communication skills
- Strong organizational skills
Benefits
- Annual Salary Range: $43,890 - $71,320
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