Clinical Research Coordinator - Tucson, AZ
15 hours ago

Job description
Posting Number
req25238
Department
UAHS Brain Science
Department Website Link
Location
Tucson Campus
Address
Tucson, AZ USA
Position Highlights
The Center for Innovation in Brain Science (CIBS) is an all brains on deck" research environment designed for highly-integrated, collaborative research through innovative team science. With expertise spanning discovery, translational and clinical science, we are addressing complex issues across four age-associated neurodegenerative diseases. The Center for Innovation in Brain Science (CIBS) is seeking a Clinical Research Assistant who will be passionate about innovation and positively impacting the quality of life for people with neurodegenerative diseases.
This position will offer an opportunity to work in a challenging and enriching role by supporting faculty engaged in mission-driven, innovative, and important research and application that will potentially impact the lives of real people and their families. The Clinical Research Assistant will assist in the overall conduct of clinical trials and will work closely with the University of Arizona/CIBS Principal Investigators, Clinical Trial Team and Research Coordinators. This position will assist with clinical trial activities, including recruitment of potential study participants, monitoring study databases and wearables, transporting study supplies to the clinical site, submit IRB applications, and other research activities.
Outstanding U of A benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; U of A/ASU/NAU tuition reduction for the employee and qualified family members; retirement plans; access to U of A recreation and cultural activities; and more
The University of Arizona has been recognized for our innovative work-life programs.
Duties & Responsibilities
- Assist in recruitment of study participants and coordinate community outreach events for the clinical trials.
- Explain trial to participants and be able to respond to any questions they could have on the pre-screening process.
- Screen and enrolls study participants who meet research criteria.
- Conduct clinical trial study visits.
- Obtains medical histories and conducts medical assessments of clinical trial subjects, including symptom management with appropriate referral.
- Creates treatment plans and serves as an information resource for trial subjects.
- Performs physical exams, including assessing vital signs and administering prescribed medications.
- Conducts adverse event assessment and provides recommendations to Principal Investigator or physicians.
- Ensures proper collection, processing, and handling of specimens.
- Collect study specimens and store following study SOPs.
- Prepare and ship laboratory specimens.
- Reviews study supply inventory to ensure site has adequate inventory of all study supplies.
- Prepare study kits.
- Ship study supplies to clinical sites.
- Conduct source data verification.
- Academic research, literature searches related to CIBS areas of interest (women's health, Alzheimer's Disease, menopause).
- Provides direct patient care involving assessment, diagnosis and administration of medicine. Assesses and monitors patient health.
- Prepares, coordinates and/or maintains all regulatory documentation.
- Submits study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor.
- Assist clinical research team with administrative tasks when necessary.
- Communicate timelines and/or impact of approvals to clinical research team.
- Actively participate in team meetings by scheduling and preparing agendas and minutes.
- Perform other duties as assigned.
- May travel to clinical sites to conduct site data verification.
Knowledge, Skills and Abilities:
- Excellent communication skills with demonstrated ability to move people and processes forward.
- Ability to work in a fast paced, dynamic team environment with changing priorities.
- Ability to interact professionally and effectively with investigators, sponsors, and cross-functional teams.
- Ability to appropriately deal with highly sensitive and confidential information.
- Highly organized, detail oriented, and able to work independently.
- Proficient with MS office (e.g., Outlook, Word, Excel and PowerPoint), MS Windows, audio/video
equipment, and online collaboration tools (e.g., Google Docs, Dropbox, OneDrive, Smartsheets). - Work well under compressed deadlines.
- Willingness to adjust schedule to work weekend and evening hours when necessary.
This job posting reflects the general nature and level of work expected of the selected candidate(s). It is not intended to be an exhaustive list of all duties and responsibilities. The institution reserves the right to amend or update this description as organizational priorities and institutional needs evolve.
Minimum Qualifications
- Bachelor's degree or equivalent advanced learning attained through professional level experience
required. - Minimum of 3 years of relevant work experience, or equivalent combination of education and work
experience.
Preferred Qualifications
- Demonstrated experience applying clinical research regulatory requirements, such as Good Clinical Practice (GCP) and HIPAA guidelines.
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
$53,039-$66,299
Compensation Type
salary at 1.0 full-time equivalency (FTE)
Grade
7
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.
The Grade Range represent a full range of career compensation growth over time. The university offers compensation growth opportunities within its career architecture. To learn more about compensation, please review our Applicant Compensation Guide and our Total Rewards Calculator.
Career Stream and Level
PC2
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
Target Hire Date
Expected End Date
Contact Information for Candidates
Gloria Bloomer I
Open Date
2/20/2026
Open Until Filled
Yes
Documents Needed to Apply
Resume and Cover Letter
Special Instructions to Applicant
Notice of Availability of the Annual Security and Fire Safety Report
In compliance with the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act (Clery Act), each year the University of Arizona releases an Annual Security Report (ASR) for each of the University's campuses. These reports disclose information including Clery crime statistics for the previous three calendar years and policies, procedures, and programs the University uses to keep students and employees safe, including how to report crimes or other emergencies and resources for crime victims. As a campus with residential housing facilities, the Main Campus ASR also includes a combined Annual Fire Safety report with information on fire statistics and fire safety systems, policies, and procedures.
Paper copies of the Reports can be obtained by contacting the University Compliance Office
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