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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Study Coordination 

• Participate in protocol development by reviewing potential protocols, informed consent documents, and evaluate their effect on standard clinical research procedures.
• Screening and Enrolling Participants: Assess patient eligibility based on study protocols.
• Recruit study participants, schedule appointments, interview and evaluate potential participants to ensure they meet eligibility requirements.
• Informed Consent: Explain the study to participants, obtain informed consent, and address concerns.
• Visit Scheduling: Coordinate patient appointments, procedures, and follow-ups.

Patient Care and Clinical Assessments:

• Monitoring Participant Health: Regularly assess and record vital signs, lab results, and adverse events.
• Administering Treatments/Interventions: Provide study-related treatments or interventions in accordance with the protocol. Coordinate and/or perform physical assessments required by protocol. Perform lab draws and give injections where an RN license is required.
• Patient Support: Offer guidance and assistance throughout the trial process.

Data Collection and Documentation 

• Document medical data in patient record. Maintain original data related to the trial for audits and reviews.
• Assist physician and/or principal investigator in writing manuscripts for publication and/or presentation of materials at conferences.
• Data Entry and record keeping: Enter data into electronic databases, ensuring accuracy and compliance with study timelines. Maintain detailed records of patient data, adverse events, and study outcomes.

Regulatory Compliance and Reporting

• Ensure all study activities are compliant with IRB protocols, FDA regulations, and Good Clinical Practice (GCP) guidelines.
• Adverse Event Reporting: Report and document adverse events and protocol deviations promptly.
• Monitoring Visits: Prepare for sponsor or regulatory audits, managing records and communication.

Collaboration and Communication 

• Teamwork: Collaborate with principal investigators, other nurses, coordinators, and healthcare providers. Actively participate in clinical research team meetings.
• Training: Assist in training other staff on study procedures or protocol amendments. Train, oversee, and provide current patient information to nurses and other health care personnel in order to assure comprehensive patient care.
• Patient Liaison: Serve as the primary contact between participants and the study team.  Evaluate and develop patient educational materials and give patient and/or family members instructions on drug administration and other medical information.
  
  
  

Knowledge, Skills, and Abilities:

• Excellent written and verbal communication skills.
• Knowledge of the principles, practices and techniques of clinical/translational research skills.
• Motivated to provide high quality, compliant research.

• Minimum of five (5) years of relevant work experience.
• Bachelor's degree or equivalent advanced learning attained through professional level experience required. In addition to the education and experience minimum qualifications, RN licensure and graduation from an accredited nursing program required.

College of Medicine-Phoenix, Office of Human Resources

HR-PHX@arizona.edu

Application: The online application should be completed in its entirety. Blank or missed information may be considered an incomplete submission.

Letter of Interest: Should clearly indicate how your skills and professional employment experience meet the Minimum and the Preferred qualifications (if applicable).