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Human Research Participant Protection Quality Improvement Coordinator at University of Oklahoma in Oklahoma City, Oklahoma

Posted in Management 30+ days ago.

Type: Full-Time





Job Description:

Responsible for assisting with the facilitation of the Human Research Participant Protection (HRPP) Quality Improvement Program including activities such as study site evaluations, internal monitoring, data collection, quality performance improvement initiatives, coordination, and investigating complaints.

Duties:



  • Provide support and assistance to HRPP and University officials regarding quality activities related to human subject research.



  • Organizes and performs research records and study site reviews to ensure compliance with IRB approved research, AAHRPP accreditation standards and human research regulations.



  • Assists with various quality performance improvement initiatives, including assisting the HRPP director in identifying potential areas for improvement, and recommending appropriate interventions to improve outcomes.



  • Assists with achieving and maintaining the standards for AAHRPP accreditation and compliance with regulatory agencies.



  • Coordinates various mechanisms in support of the goal of the HRPP Quality Improvement Program.



  • Assists in the identification and and resolution of quality of human research, risk management, and participant safety through the use of incident reports, complaints, chart reviews and site evaluations.



  • Works with research investigators, study staff, HRPP staff, and IRB to resolve issues.



  • Assists the Institutional Review Board, and other committees as applicable.



  • Assists with the planning, coordination, and participation of HRPP and IRB directed education initiatives.



  • Performs a variety of duties associated with the HRPP Quality Improvement Program to include the collection and analysis of data, measure and evaluate HRPP and IRB review processes, and quality of HRPP and IRB review.



  • Performs various duties as needed.


Required Education: Bachelor's Degree


  • 24 months IRB, research administration, or clinical research experience

 Equivalency/Substitution: 48 months related clinical or IRB experience in lieu of the Bachelor Degree for a total of 72 months experience

Skills:


  • Knowledge of computer applications, data management and;or analysis.

  • Proficiency in Microsoft Office Suite (Word, Excel, Access, PowerPoint, and Outlook), Adobe Acrobat, and IDX and;or Meditech. 

  • Strong verbal and written communication skills. Strong organizational skills.

Certifications: Successful completion of the IRB Professional Certification required after two years.  

 

Working Conditions: Standard office environment

 


Equal Employment Opportunity Statement

The University of Oklahoma, in compliance with all applicable federal and state laws and regulations, does not discriminate on the basis of race, color, national origin, sex, sexual orientation, genetic information, gender identity, gender expression, age, religion, disability, political beliefs, or status as a veteran in any of its policies, practices, or procedures. This includes, but is not limited to, admissions, employment, financial aid, housing, services in educational programs or activities, and health care services that the University operates or provides.  

 

Diversity Statement  

The University of Oklahoma is committed to achieving a diverse, equitable, and inclusive university community by recognizing each person's unique contributions, background, and perspectives. The University of Oklahoma strives to cultivate a sense of belonging and emotional support for all, recognizing that fostering an inclusive environment for all is vital in the pursuit of academic and inclusive excellence in all aspects of our institutional mission.





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