Senior Human Research Protection Program (HRPP) Administrator-4
Core
Administers and implements the Human Research Protection Program (HRPP) and Institutional Review Board (IRB) policies to ensure compliance with federal regulations and ethical standards for biomedical and behavioral human subjects research.
Role type
Senior HRPP Administrator
Builds
Compliance with federal/state regulations and institutional policies for human subjects research
Domain
Academic/Clinical Research Ethics & Compliance
Required skills
Human subjects research regulations, FDA regulations, protocol review, IRB meeting support, electronic IRB systems, SOP implementation
Preferred skills
CIP certification, clinical trial management, clinical trial registration, clinical trial results reporting
Technologies
Electronic IRB submission systems, Microsoft Office, Google platforms, Adobe
Responsibilities
Conduct non-committee reviews, prepare IRB meeting agendas and materials, take minutes, advise IRB members on regulations, maintain knowledge of federal/state laws and institutional policies
Seniority
Senior, hands-on IC