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Job ID: 141126

HRPP Administrator
University at Buffalo, The State University of New York

Date Posted Apr. 10, 2020
Title HRPP Administrator
University University at Buffalo, The State University of New York
Buffalo, NY, United States
Department Office of Research Compliance
Application Deadline Open until filled
Position Start Date Available immediately
  • Classified Staff
  • Research/Technical/Laboratory

The Human Research Protection Program (HRPP) Administrator will manage the privileged and confidential institutional review and approval process of all proposed research activities involving human subjects to protect their safety, rights, and welfare. Under administrative direction, the HRPP Administrator will serve as a member, with vote, on the Institutional Review Board (IRB); 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 preparation of applications and consent forms; and review and approve administrative and procedural modifications of applications. This position reports to the Director of Research Compliance.

Primary Duties and Responsibilities:
o Serves as a voting member of the IRB, and functions as a designated reviewer for exempt and expedited reviews.
o Interpret and apply federal and state laws, regulations, institutional policies, and guidelines to protect human subjects and to ensure institutional compliance.
o Ensures research activities are carried out in a manner that is compliant with all federal, state and local requirements by providing direction on promoting and maintaining required compliance.
o Provide regulatory, ethical, and method advice to individual faculty, staff, and students in preparation of applications for research proposals involving human subjects and consent documents.
o Draft correspondence that conveys IRB deliberations and contingencies for approval of research activities involving human subjects.
o Assist in program development, implementation, and evaluation.
o Establish and maintain oneself as a professional expert and resource to the organization, patients, families and the Community. Participate in appropriate professional organizations and continuing education programs.
o Other duties as assigned.

University at Buffalo is an affirmative action/equal opportunity employer and, in keeping with our commitment, welcomes all to apply including veterans and individuals with disabilities.

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