Outstanding UA benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; UA/ASU/NAU tuition reduction for the employee and qualified family members; state and optional retirement plans; access to UA recreation and cultural activities; and more!

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• Project Management: Identify key resources, establish project organization structure and manage project team by providing the direction required for meeting the project objectives/deliverables. Manage day-to-day project activities. Clarify roles, responsibilities and deliverables for all study protocols and CRU staff.
• Provide regular status reports to the Medical Director, Director of Operations, and PIs. Identify needs and work with A2DRC leadership to ensure appropriate systems/technologies are in place to support project requirements.
• Create and distribute internal and external communications pertaining to critical project activities, deadlines, deliverables, and overall project progress.
• Manage written and verbal communications with all stakeholders. Keep team members appropriately informed.
• Mentor and Develop: Supervise a clinical trial research team of 5-10, assuring that all team members understand their roles, responsibilities and priorities among project activities.
• Train and mentor all CRU personnel, ensuring all certifications are maintained.
• Manage personnel resources and provide professional development opportunities for all. Facilitate group discussions.
• Research and Analysis: Provide back-up to CRCs for all active protocols/study visits.
• Direct study data collection and oversee data entry.
• Monitor enrollment goals and modify recruitment strategies as necessary. Upon request, supply information to PIs and Center leadership to develop progress reports, posters, manuscripts, and abstracts.
• Compliance: Ensure that the CRU staff adhere to all necessary Standard Operating Procedures and Good Clinical Practice.
• Participate in continuing education on latest government, state, UA and hospital regulations of research activities by attending research-related seminars and monthly meetings offered by those entities.
• Work with UAHS and A2DRC Regulatory teams to prepare and process IRB, FDA and sponsor regulatory document filings. Upon request supply information and support for trial start up and closeout procedures.
• Travel may be required.

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