Manager Human Subject Protection Program-(CLI000210)
Work location:OSF Healthcare System - Peoria, IL61603
Reporting to the Director, Research Administration is responsible for developing, managing, and evaluating policies, procedures that ensure compliance with all state, and federal regulations governing human subject research at OSF Healthcare System. This includes monitoring changes in regulation and policies that relate to human research protection and overseeing all aspects of the HSPP.
Bachelor’s degree and 10+ years of related experience required, 5years management/leadership experience required.
Demonstrated knowledge of human subject protection and related regulations normally acquired through employment with an Institutional Review Board (IRB).
Knowledge of research regulations, HIPAA (regarding human subjects), and familiar with current NIH, DHHS, OHRP, and FDA guidelines.
Certification as Certified IRB Professional (CIP) required or expected within 1 year.
Must be highly proficient in all Microsoft programs.
Understanding of issues pertinent to Academic Medical Centers and clinical research issues that surround such activities.
Analytical abilities necessary in order to prepare audit and monitoring plans/reports; respond to problems by identifying and recommending appropriate corrective action; develop and administer sound policies, procedures; and organize and oversee work of subordinates.
Master’s degree in related field
Familiarity with IRB software and/or Clinical Trial Management System
Clinical Research at OSF:
From the time of their very first patient in a small home on Adams Street in Peoria, The Sisters of the Third Order of St. Francis have stayed true to their promise to God to never turn away anyone He sent to them for care. Over the years that founding promise has fueled the OSF HealthCare Mission “…to serve with the greatest care and love.”
Clinical Research helps OSF HealthCare to serve patients with complex needs in a compassionate way. Those participating in clinical research may do so because no other treatment has worked or because they see the possibility of restored health through the investigational treatments of a clinical study.Others participate because they want to contribute to medical science and help doctors and researchers find better ways to help others. All clinical research participants are closely monitored by the principal investigators conducting the study.
Many of our OSF Mission Partners and collaborating institutions are leading research efforts. To learn more, please visit the links below:
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