Indianapolis, Indiana
Oklahoma City, Oklahoma
Nashville, Tennessee
Bloomington, Indiana
Chicago, Illinois
Laurel, Maryland
Posted: 13-Feb-25
Location: Phoenix, Arizona
Type: Full Time
Categories:
Internal Number: 910560
Position Summary
The ideal candidate will have experience making QI/NHSR/exempt determinations, providing investigator support, working independently, and have a growth mindset.
Remote available in most states. Please send resume and cover letter.
This position supervises the development, implementation, and evaluation of clinical research trials to ensure consistency with all IRB policies and procedures; coordinates resource requirement and utilization to ensure compliance with required federal, state, funding source, and all other applicable governing regulations, requirements, and standards. This position also provides regulatory, ethical and methodological guidance to investigators and coordinators to prepare applications for research proposals involving human subjects and provides consultation to IRB members and institutional officials regarding federal regulations and institutional policy.
Education
- Bachelors degree in a related field (Preferred)
Experience
- Four (4) or more years of experience in human research protection administration (Required)
- Experience with applicable federal and state guidelines and regulations (Preferred)
- Four (4) or more years of experience as an IRB Coordinator (Preferred)
Certifications
- Certification in IRB Management (CIM) or Certified IRB Professional (CIP) OR qualified to sit for exam and pass exam prior to employment start date (Required)
