Clinical Research Coordinator

Clinical Research Coordinator

Posting Number
: req
25238

Location
:
Tucson Campus, Tucson, AZ USA

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. CIBS is seeking a Clinical Research Coordinator who will be passionate about innovation and positively impacting the quality of life for people with neurodegenerative diseases.

This position offers an opportunity to work in a challenging and enriching role by supporting faculty engaged in mission‑driven, innovative, and important research that may impact the lives of real people and their families. The Clinical Research Coordinator 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.

Responsibilities include recruitment of potential study participants, monitoring study databases and wearables, transporting study supplies to the clinical site, submitting IRB applications, and other research activities.

Outstanding U of A benefits: 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.

For more information about working at the University of Arizona and relocation services, .

• Assist in recruitment of study participants and coordinate community outreach events for the clinical trials.
• Explain trial to participants and respond to any questions during the pre‑screening process.
• Screen and enroll participants who meet research criteria.
• Conduct clinical trial study visits.
• Obtain medical histories and conduct medical assessments of clinical trial subjects, including symptom management with appropriate referral.
• Create treatment plans and serve as an information resource for trial subjects.
• Perform physical exams, including assessing vital signs and administering prescribed medications.
• Conduct adverse event assessment and provide recommendations to Principal Investigator or physicians.
• Ensure proper collection, processing, and handling of specimens.
• Collect study specimens and store following study SOPs.
• Prepare and ship laboratory specimens.
• Review 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).
• Provide direct patient care involving assessment, diagnosis, and administration of medicine. Assess and monitor patient health.
• Prepare, coordinate and/or maintain all regulatory documentation.
• Submit 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 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.

• 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 (Outlook, Word, Excel and PowerPoint), MS Windows, audio/video equipment, and online…