Clinical Research Coordinator II

Position Highlights

The purpose of this position is to coordinate and participate in the conduct and management of complex clinical research studies under the direction of departmental research leadership and Principal Investigators. The role applies knowledge of clinical research principles to support compliance with study protocols, regulatory requirements, and institutional policies. Responsibilities include all aspects of clinical trial conduct, including participant recruitment, informed consent, study procedures, data collection, regulatory management, and study close-out activities.

Visa sponsorship is not available for this position.

Outstanding U of A 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 retirement plan; access to UA recreation and cultural activities; and more!

• Coordination of study visits and study procedures. Maintaining regulatory and study documentation.
• Creating source documents, study specific training in accordance with study protocols and Good Clinical Practice (GCP) guidelines.
• Perform participant pre-screening, screening, recruitment, enrollment, and informed consent.
• Conduct study visits and clinical procedures as required by protocol.
• Maintain accurate and complete source documentation and study records.
• Develop study-specific tools including source documents, visit checklists, and training materials.
• Ensure maintenance and organization of regulatory documentation, including IRB submissions, continuing reviews, protocol amendments, and reporting requirements.
• Monitor and report adverse events, serious adverse events, and protocol deviations in accordance with institutional and sponsor requirements.
• Perform data collection, entry, management, and quality control checks to ensure accuracy and completeness of study data.
• Resolve data queries and maintain research databases (e.g., REDCap or equivalent systems).
• Work closely with Principal Investigators to coordinate and execute all aspects of multiple clinical trials.
• Collect, process, and ship biological specimens according to protocol requirements and ensure proper chain of custody and storage conditions.
• Maintain study supplies, inventory, and equipment required for research operations.
• Communicate effectively with study sponsors, IRB, clinical teams, laboratories, and other stakeholders to ensure study compliance and efficiency.
• Participate in study initiation, monitoring visits, audits, and close-out activities as required.
• Responsibilities are subject to change based on departmental priorities, study requirements, regulatory obligations, and operational needs.

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.

• Research exposure/experience preferred.