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Birch Regulatory Advisor
Brown University
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Job Description:
About Brown
Brown University is a leading research university distinct for its student-centered learning and deep sense of purpose. Our students, faculty and staff are driven by the idea that their work will have an impact in the world. Brown University offers a flexible work/life balance; summer hours, winter break and a comprehensive Benefits package including time off, annual paid holidays; benefits offerings including health, dental, vision, tuition assistance, retirement, wellness, employee discounts and more. To learn about Brown University's benefits, visit the University Human Resources web page here for further information.
About the Opportunity
Brown HRPP is growing!
As part of the BIRCH initiative, Brown will soon be the main HRPP and Institutional Review Board (IRB) of record for Brown, Lifespan and Care New England health systems, and our HRPP is growing to meet this increased responsibility. The HRPP will be responsible for approximately 4000 protocols across eight institutions, spanning every area of academic and clinical research.
The Regulatory Advisor serves as a central resource for researchers proposing to conduct biomedical, social or behavioral research involving human subjects. Working closely with researchers and the Human Research Protections Program (HRPP) Office, the Regulatory Advisor assists in the development, completion, and submission of the human subjects study application and other required documentation to the Institutional Review Board. This position will work independently with researchers providing advice regarding the design of studies and help translate research ideas into study protocol submissions that meet all IRB regulatory and ethical requirements. This role will also work closely with the Research Training Office to develop educational materials to assist investigators who are new to human subjects research understand compliance context related to clinical, social, and behavioral research, and navigate the IRB submission requirements and process.
This position will play a critical role in educating and supporting the research community on managing study related regulatory requirements, such as setting up regulatory binders, as needed, managing the ClinicalTrials.gov registration process, and compliance with annual review requirements and reports.
Education and Experience
Required:
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