IRB Coordinator

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The IRB Coordinator/Program Manager manages the review and approval processes for all research activities to protect the patient’s safety, rights, and welfare in accordance with Federal Regulations, IRB Policies and Standard Operating Procedures, and SCL Health Policies. 


Under administrative direction, the IRB administrator will serve as a member on the Institutional Review Board; perform highly complex duties to facilitate the review and approval process, such as use of independent judgment in interpreting and applying relevant federal and state laws, regulations, and institutional policies and guidelines; conduct literature reviews and prepare reports on scientific topics and on regulatory precedent and changes; instruct IRB chairs, members, and researchers on the regulations and ethical principles essential to the review process; provide training and advice to faculty, staff, and student researchers on the regulations and on the preparation of applications and consent forms; review and approve administrative and procedural modifications of applications; and manage IRB operations and IRB Coordinators.




  • Bachelor’s Degree in Health/Social Sciences (or related field) or has the equivalent combination of training, experience, and CIP (Certified IRB Professional) Certification. 
  • CIP Certification within one year of eligibility if not certified when assuming role. 
  • A minimum of three years’ experience involving human subject’s research, performing a majority of the duties listed above, and interacting with investigators and regulatory agencies in the area of human subject research.
  • Applicant must be proficient in the use of personal computers, Microsoft Word and Excel, and the internet.  Experience with IRB specific software preferred. 
Organization: Corporate, Various Locations
Primary Location: CO-Denver/Boulder/Surrounding Areas-Denver
Department: SYS-Research
Schedule: Full-time
Shift: Day Shift
FTE: 1.0
Job Number: 17008802
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