Philadelphia, PA10 days ago
p>Essential duties: - Conducting review of IRB protocol submissions, continuing reviews, and amendments to approved studies;
- Assisting Principal Investigators (PIs) in developing and submitting protocols and informed consent forms by offering expertise in study design, regulations regarding human subjects research, and navigating our submission process;
- Identifying issues or concerns and working with the PI to ensure that the issues are resolved prior to the IRB committee meetings, thereby decreasing the length of the IRB review process of submissions;
- Developing training tools for the research community to provide guidance on the preparation of IRB submissions;
- The IRB Program Analyst I must maintain up-to-date knowledge of state and federal regulations as well as policies, guidelines and ethical codes related to the protection of human subjects in research.
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