The Clinical Research Coordinator I (CRC-I) will provide dedicated research support for clinical trials focused on complex respiratory illness (e.g., allergy, asthma, COPD, and cystic fibrosis). The CRC-I will conduct all manner of assessments related to research in the Asthma and Airway Disease Research Center (A2DRC), including pulmonary function testing and collection/processing of samples. This position is responsible for adhering to all regulatory matters associated with the conduct of clinical trials and assisting with the design or modification of study source documents.

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; retirement plans; access to UA recreation and cultural activities; and more!

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• Support all day-to-day activities involved with research protocols: prepare and ship laboratory specimens; assist with recruitment, scheduling and consenting research participants; assist CRC leads with data collection and data entry (adhering to proper protocols); prepare study materials for each study protocol; etc.
• Under direction of the study lead and/or Manager perform study related procedures: Administration of questionnaires; Phlebotomy; Nasal swabs/brushings; Sputum induction: conducting pulmonary function testing.
• Assist lead coordinators in contacting the investigational pharmacy to order, collect, and distribute the appropriate study pharmaceuticals, as needed. Maintain drug accountability and destruction logs, as required. Access Banner EMR and have access to Cerner, as needed to confirm inclusion/exclusion of research participants and to log AE's/SAE's.
• Assist the regulatory team with monitoring visits: Prepare monitoring room, prior to monitoring visits, with study materials, escort monitor to other areas, provide requested documents to monitor throughout the visit.
• Under direction of the Lead CRC, maintain study binders and assist with any related audits.

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

• Direct experience in Human Subject Research.
• Experience with both adult and pediatric research patients/subjects