Clinical Research Coordinator
Listed on 2026-01-12
-
Healthcare
Clinical Research -
Research/Development
Clinical Research
Overview
This clinical research coordinator position is responsible for coordinating a clinical trial patient through all protocol-required procedures. This includes, but is not limited to, obtaining consent, screening, collecting and entering data, and performing follow-up for all patients enrolled in assigned clinical trials. The coordinator serves as the liaison between regulatory, research, clinic, clinical faculty, and research sponsor staff to carry out the required events outlined in the protocol calendars, including data entry.
The coordinator is involved in carrying out the clinical research protocols from the time the project is initiated through study closure. It is expected that this person will have, or develop, a knowledge base of the assigned disease areas and of clinical research coordinator responsibilities in the sleep, circadian, and mental health areas.
Note:
The University of Arizona benefits language and related information are provided for context and are kept for historical accuracy in the posting.
- Administer clinical tests and questionnaires as part of clinical research protocols (assessments of sleep, circadian rhythms, mental health, cognitive functioning).
- Data entry for clinical study protocols and preparation of reports.
- Prepare documents for submission to Research Intake and IRB, including protocols and consent forms, working with faculty, residents, external sponsors and internal departments.
- Assist in research coordination to include administrative support schedule coordination, intake and maintaining records/files.
- Since some research activities will take place during evenings and/or weekends, a willingness to occasionally work those hours is required.
- Conduct and review recruitment activities, including community-based recruitment and activities in coordination with Psychiatry clinics.
- Work closely with participants to assist them through the various protocol elements of the research study.
- Assist with administrative tasks associated with the program. This includes assistance with all various administrative tasks within the research program with a concentration surrounding purchasing and receipts.
- Demonstrated strong interpersonal, communication, and problem-solving skills.
- Excellent organizational skills.
- Attention to detail.
- Ability to multitask using time management skills.
- Comfortable with navigating electronic databases.
- Other tasks as assigned.
- Bachelor's degree or equivalent advanced learning attained through experience required.
- Up to 1 year of relevant work experience may be required.
- Experience working or volunteering directly with patients in a healthcare setting, or human subject experience.
- Experience working with people with mental health conditions and/or sleep or circadian research.
- Comfort in administering sensitive mental health assessments.
- CCRC training.
- Experience with federal regulation adherence.
FLSA Exempt
Full Time/Part Time Full Time
Number of Hours Worked per Week 40
Job FTE 1.0
Work Calendar Fiscal
Job Category Research
Benefits Eligible Yes - Full Benefits
Rate of Pay $47,356.00 - $59,195.00
Compensation Type salary at 1.0 full-time equivalency (FTE)
Grade 6
Compensation Guidance The Rate of Pay Field represents the University of Arizona’s good faith and reasonable estimate of the range of possible compensation at the time of posting. The University considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate’s work experience, education/training, key skills, and internal equity.
Career Stream and Level PC1
Job Family Clinical Research
Job Function Research
Type of criminal background check required: Name-based criminal background check (non-security sensitive)
Number of Vacancies 1
Open Date 10/24/2025
Open Until Filled Yes
Documents Needed to Apply Resume and Cover Letter
Special Instructions to Applicant
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Paper copies of the Reports can be obtained by contacting the University Compliance Office at cleryact.
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