The Sarver Heart Center invites applicants to apply for a Clinical Research Coordinator I position to assist in the coordination of clinical research projects by screening, interviewing, recruiting, and performing study visits. This will require communicating professionally with physicians, hospital partners, and sponsors regarding studies; providing cross coverage of duties as described below at satellite and partner sites as assigned; processing medical samples; and providing back up support for other research coordinators and protocols as requested. Weekend and evening departmental support may be required to meet study protocol requirements.

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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• Screen, recruit, and enroll participants for medical studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met.
• Evaluate potential study participants to ensure they meet eligibility requirements, instruct study participants concerning research protocol, and complete the patient informed consent procedure.
• Schedule and/or perform medical testing per protocol such as drawing blood, vital signs, EKGs, etc., includes processing and packaging of laboratory samples for shipment.
• Assess participants during clinic visit; perform initial review of study lab results; determine if patient is experiencing side effects or other problems; and notify principal investigator if problems arise.
• Complete case report forms for each study participant and document medical data in the patient record and sponsor database. Ensure case report forms or other data collection/tracking tools are created if not provided by sponsor.
• Participate in sponsors site visits for assigned studies.
• Occasional out-of-state travel may be required for sponsor training.

• Bachelor's degree or equivalent advanced learning attained through experience required.
• One (1) year of relevant work experience required.

• One year of experience in interaction with patients in a clinical setting and/or clinical trial research experience.