Research Compliance Coordinator-Senior (Pediatrics Research)

University of Texas Health Science Center San Antonio, United States

Updated: over 2 years ago
Location: San Antonio, TEXAS
Deadline: The position may have been removed or expired!

Job Summary:

The focus of this role will be on regulatory protocols and structure. Under limited supervision, responsible for developing and presenting educational and research materials to compliance officials, research staff, regulatory committee members, and the research community to increase awareness of, and compliance with human subject, laboratory animal, or biologically infectious agent regulations. May lead or mentor lower-level team members.

 

Job Duties:

  • Ensures the institution's compliance with policies regarding the use of human subjects, laboratory animals or biologically infectious agents in research.
  • Develops and implements compliance program components including protocol and consent form review, record keeping, monthly and annual reporting, program evaluation and other compliance issues that meet the regulations and the institution's policies and procedures.
  • Provides education, advice and assistance to compliance officials, regulatory committee members, principal investigators, research staff, and office staff to increase awareness of, and compliance with human subject regulations; integrates lessons learned into educational materials.
  • Evaluates processes and policies, and recommends changes; impacts budgeting, controlling costs, planning, scheduling, and procedural change.
  • Secures the cooperation of and coordinates with applicable institutional offices, affiliated institutions, or regulatory/accrediting agencies.
  • Assists in the preparation of information and reports for grant submissions and or budget analysis.
  • Performs all other duties as assigned.

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    Education:

    • Bachelor's degree in a scientific related field or equivalent is required.

     

    Experience:

    • Three (3) years of related experience is required.
    • The ideal candidate will have experience with start-up applications for grants and clinical trials.

     

    Additional Licenses and Certifications:

    • Certification in an applicable field (e.g., CIP, CPIA, CCRC/CCRA, or CCRP) is preferred.

     


    Additional Information

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