Job Summary
A company is looking for a Clinical Research Coordinator II.
Key Responsibilities
- Coordinates research projects, including patient/participant interaction and data management
- Maintains regulatory documentation and ensures compliance with industry standards and protocols
- Assists in developing research studies and protocols, and prepares necessary documentation for Institutional Review Board (IRB) submission
Required Qualifications
- Bachelor's Degree in a medical or science-related field
- Two years of clinical research experience
- Additional years of experience or an advanced degree may substitute for education or experience
- BLS and CPR AED certifications may be required based on study protocols
- ACRP or SOCRA certification is preferred
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