Research Compliance Administrator II

The Department of Psychiatry seeks a Research Compliance Administrator II to support various clinical trials involving several psychiatric indications. The Research Compliance Administrator II will work closely with the study staff and principal investigator to facilitate the clinical trials by screening participants, obtaining informed consent, recording interventions, obtaining labs and other required tests, completing case report forms, assisting with query resolution, and scheduling study participants for follow-up. The incumbent will work under limited or minimal supervision and will consult the principal investigator and management with highly unusual or complex situations. The mission of the University of Arizona - Department of Psychiatry is to foster excellence in psychiatric patient care, research, and technical innovation. We strive to be leaders and role models of excellence, innovation, and caring in all that we do, and we are committed to investigating the next generation of psychiatric interventions for our patients.

• Visa sponsorship is not available for this position.

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• Provides regulatory advice in the areas of research compliance and safety.
• Develop and/or advise on research compliance procedures, processes, and policies.
• Prepare, coordinate and maintain regulatory compliance and related documentation required by regulatory agencies or sponsors. Review and track regulatory documentation.
• Prepares and/or coordinates IRB submissions.
• Prepares and/or coordinates reports and updates for our funder(s).
• Works under limited or minimal supervision and consults Senior Professional with highly unusual or complex situations.
• Mentors and share knowledge with student workers and support staff.

This job posting reflects the general nature and level of work expected of the selected candidate(s). It is not intended to be an exhaustive list of all duties and responsibilities. The institution reserves the right to amend or update this description as organizational priorities and institutional needs evolve.

• Bachelor's degree or equivalent advanced learning attained through professional level experience required.
• Minimum of 3 years of relevant work experience, or equivalent combination of education and work experience.

• Experience working in pharmaceutical clinical trials preferred.
• Experience working with behavioral, cognitive, and psychological testing.
• Experience compiling datasets for funder/sponsor reporting and updates, clinicaltrials.gov, and final project reporting.
• IRB experience preferred.

Application: The online application should be completed in its entirety. Blank or missed information may be considered an incomplete submission.

Cover Letter: Should clearly indicate how your skills and professional employment experience meet the Minimum and the Preferred qualifications (if applicable).