Hrpp IRB Senior Analyst

Drug Information Association Inc La Jolla , CA 92037

Posted 2 months ago

UC San Diego Health

HRPP IRB Senior Analyst

Filing Deadline: Tue 4/28/2020

Salary Range: Commensurate with Experience


Under the direction of the Director/Deputy Director/Associate Director, the Sr. Analyst will independently manage/support the review of the Exempt and Expedite applications, in addition, when needed, may assist in the support of the six Federally mandated human subject research review committees, five Biomedical Institutional Review Boards which review research for the UCSD, and Radys Children Hospital and one Social and Behavioral Sciences Institutional Review Board that reviews research for the entire UCSD campus. The incumbent manages reviews, and other collaborative review efforts such as conflict of interest, radiation safety, biosafety committee, and facilitates and may finalize committee deliberations, when needed. As an alternate member of the Institutional Review Board, may attend assigned IRB meetings, present and summarize findings as appropriate.

The Sr. Analyst provides complex analytical and administrative support to the UCSD Human Research Protections Programs, Institutional Review Boards (Biomedical and/or Social and Behavioral), related collaborating University and external regulatory offices and UC and Non- UC IRB reliance agreements through independent reviews of incoming grants and administrative amendments to research protocols, master protocols (from sponsors), Investigator Brochures, and related documentation. In addition, the analyst will review new information impacting IRBs or related areas and will be involved in recommending process revisions and disseminating information to the VCHS, Campus Principal Investigators (PIs) and study administrative staff. May be asked to audit IRB maintained study records in accordance with HRPP standards and may perform periodic audits of the informed consent process and the approved research at the Investigator's site to ensure that the study is being conducted as required by the IRB.


  • Bachelor's Degree in related area; and/or equivalent experience/training.

  • A minimum of three (3+) or more years of IRB/regulatory experience.

  • Demonstrated strong project management experience.

  • Strong knowledge and ability to apply all relevant Federal, state, and university regulations, policies, and federal guidance documents. Thorough knowledge or demonstrated related experiences to comprehend, interpret, and apply complex regulations and legislation regarding the protection of human subjects. These include federal, state and local regulations and policies including DHHS, HHS-OHRP regulation, FDA regulations for the use of investigational drugs, biologics and devices; California law on human experimentation, other compliance agencies or directives, and university policy regarding human subject research.

  • Thorough knowledge and experience with quantitative and qualitative research design; scientific research concepts and terminology.

  • Proficiency in public speaking, and writing. Excellent interpersonal, written, and oral communications. Proven ability to compose complex correspondence (high volume, short time-lines) that is accurate, typographically and grammatically correct.

  • Conflict of Interest: Understanding of stock options, consulting agreements and other corporate documents related to research and analysis of potential conflicts of interest.

  • Thorough knowledge of informed consent process and ability to conduct audits of the process.

  • Demonstrated experience in developing training programs and materials to educate different populations to include but not limited to faculty, principal investigators, researchers, study staff, etc.

  • Expertise in clinical trials and/or behavioral sciences, investigator-initiated studies, and grant-supported research or related areas. Knowledge of the academic research and medical/scientific terminology and demonstrated ability to comprehend the research process and the various components.


  • Certified IRB Professional or Certified IRB Manager.


UC San Diego Health is the only academic health system in the San Diego region, providing leading-edge care in patient care, biomedical research, education, and community service. Our facilities include two university hospitals, a National Cancer Institute-designated Comprehensive Cancer Center, Shiley Eye Institute, Sulpizio Cardiovascular Center, and several outpatient clinics. UC San Diego Medical Center in Hillcrest is a designated Level I Trauma Center and has the only Burn Center in the county. We invite you to join our dynamic team!

Applications/Resumes are accepted for current job openings only. For full consideration on any job, applications must be received prior to the initial closing date. If a job has an extended deadline, applications/resumes will be considered during the extension period; however, a job may be filled before the extended date is reached.

UC San Diego Health is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, age, protected veteran status, gender identity or sexual orientation. For the complete University of California nondiscrimination and affirmative action policy see:

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Hrpp IRB Senior Analyst

Drug Information Association Inc