Clinical Research Coordinator I, Liver Research Institute

The Thomas Boyer Liver Research Institute is seeking applicants for a Clinical Research Coordinator I. The successful candidate will explore and discover answers to challenging questions as it relates to current and future clinical trials within the Institute. This individual will develop, facilitate, implement, evaluate, perform, administer, and oversee a wide variety of research programs or initiatives within the division, the College of Medicine - Tucson, and the community.

This position may be eligible for a flexible schedule work arrangement in conversation with the supervisor.

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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• Under the supervision of the PI, provides assistance in the coordination of Liver Clinical Trials, protocols and treatment plans and may provide additional assistance to the Clinical Research Coordinator II and/or III.
• Following detailed instructions from the PI, prepares, coordinates, and maintains regulatory study documentation including IRB submission and approval of new or revised protocols, safety reports and progress reports.
• Maintains Liver Registry REDCap database.
• Under the PI's direction, coordinates the gathering of study data and data entry.
• Screens hepatology clinics via Electronic Medical Records, with guidance from supervisor.
• Following established protocols, obtains consents and explains research protocols to study participants.
• Coordinates study appointments and performs procedures, including obtaining vitals, collection of specimens, administering medication, and assessing and monitoring patient's health, under the close supervision of the PI.
• Assists in the coordination of physical exams with the PI.
• Ensures the proper collection, processing and handling of specimens, and packaging and shipping of samples to the sponsor.
• Provides education materials and training to patients, family members, and clinical staff to assure patient safety and adherence to protocols.
• Assists PI and higher level Clinical Research Coordinator staff with sponsor monitor visits.

Knowledge, Skills, and Abilities

• Ability to handle sensitive patient information.
• Knowledge of recent advancements in clinical trials.
• Knowledge of Hep-C related diseases.
• Ability to communicate effectively with different groups and individuals.

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