University of Utah
Job Summary
The Division of Vascular Surgery at the University of Utah has an immediate opening for a Clinical Research Coordinator. This position desires a person with a strong background in clinical research.
This position will: (1) assist in facilitating the conduct of clinical research by performing research duties for Vascular Surgeon Research Investigators; (2) coordinate technical and administrative details involved in both sponsor- and physician-initiated clinical research studies; and (3) assist the Principal Investigator and study team in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures.
Responsibilities
Screen and recruit participants for clinical research studies.
Fully understand the informed consent process and obtain informed consent from eligible study participants; document the informed consent process; write informed consent documents under the supervision of the study investigator.
Attend and actively participate in study team meetings; assume leadership roles within study teams.
Schedule study visits and coordinate related facility and equipment availability.
Assess research protocols for clarity and participant safety, review inclusion/exclusion criteria, clarify concerns and questions with the Principal Investigator and sponsor.
Collect and document clinical research data such as medical history and demographics; maintain research documentation including status reports, progress notes, and participant logs to help ensure safety.
Report and track adverse events (AEs); report serious AEs to PI, IRB, and sponsor.
Review and manage clinical research study databases.
Educate staff regarding study procedures.
Document all protocol deviations, reconcile test article accountability at study closeout and prepare summary report for sponsor.
Complete, audit, correct, and relay case report forms (CRFs) to sponsor.
Assist with negotiating study contract budget and payment terms.
Maintain documents as required by FDA, ICH, GCP, and IRB regulatory guidelines.
Maintain contact with IRB and prepare and submit IRB documents.
Ensure proper collection, processing and shipment of specimens.
Help determine personnel required to complete the trial and develop the timeline for trial completion; review study related data to assure compliance with study protocol.
Work Environment Nearly continuously: Office environment. Seldom: infectious disease exposure, oils (there is air or skin exposure to oils or other cutting fluids).
Physical Requirements Nearly continuously: hearing, listening, talking. Often: repetitive hand motion (such as typing), walking, standing, sitting. Seldom: bending, reaching overhead.
Minimum Qualifications
Bachelor’s degree in a health sciences or related field or equivalency (one year of education can be substituted for two years of related work experience) with two years professional research experience and completion of University RATS Clinical Certification within one year of hire required.
Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills also required.
Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; and the ability to function independently.
Departments may require IRB CITI Course or IATA DGR training within a specified timeframe.
Departments may prefer a nursing degree for this position, which requires the incumbent to have two years related experience and possess a nationally recognized research compliance certification.
Position is patient-sensitive and must fulfill all associated requirements. All patient-sensitive employees must be immunized according to CDC standards and hospital policy (limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations).
Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.
Preferences
Master’s degree in a health science field.
Credentialing as an Association of Clinical Research Professionals (ACRP) Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Associates (SOCRA) Certified Clinical Research Professional (CCRP).
Special Instructions Requisition Number: PRN43953B
Full Time or Part Time?: Full Time
Work Schedule Summary
Department: 00917 – Vascular Surgery Development
Location: Campus
Pay Rate Range: $39,300 to $72,700
Close Date: 4/6/2026
Open Until Filled
To apply, visit
https://utah.peopleadmin.com/postings/194544
Equal Opportunity Employer University of Utah is an equal opportunity employer and welcomes diversity in the workplace. Applications will be considered in accordance with all applicable laws and regulations.
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This position will: (1) assist in facilitating the conduct of clinical research by performing research duties for Vascular Surgeon Research Investigators; (2) coordinate technical and administrative details involved in both sponsor- and physician-initiated clinical research studies; and (3) assist the Principal Investigator and study team in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures.
Responsibilities
Screen and recruit participants for clinical research studies.
Fully understand the informed consent process and obtain informed consent from eligible study participants; document the informed consent process; write informed consent documents under the supervision of the study investigator.
Attend and actively participate in study team meetings; assume leadership roles within study teams.
Schedule study visits and coordinate related facility and equipment availability.
Assess research protocols for clarity and participant safety, review inclusion/exclusion criteria, clarify concerns and questions with the Principal Investigator and sponsor.
Collect and document clinical research data such as medical history and demographics; maintain research documentation including status reports, progress notes, and participant logs to help ensure safety.
Report and track adverse events (AEs); report serious AEs to PI, IRB, and sponsor.
Review and manage clinical research study databases.
Educate staff regarding study procedures.
Document all protocol deviations, reconcile test article accountability at study closeout and prepare summary report for sponsor.
Complete, audit, correct, and relay case report forms (CRFs) to sponsor.
Assist with negotiating study contract budget and payment terms.
Maintain documents as required by FDA, ICH, GCP, and IRB regulatory guidelines.
Maintain contact with IRB and prepare and submit IRB documents.
Ensure proper collection, processing and shipment of specimens.
Help determine personnel required to complete the trial and develop the timeline for trial completion; review study related data to assure compliance with study protocol.
Work Environment Nearly continuously: Office environment. Seldom: infectious disease exposure, oils (there is air or skin exposure to oils or other cutting fluids).
Physical Requirements Nearly continuously: hearing, listening, talking. Often: repetitive hand motion (such as typing), walking, standing, sitting. Seldom: bending, reaching overhead.
Minimum Qualifications
Bachelor’s degree in a health sciences or related field or equivalency (one year of education can be substituted for two years of related work experience) with two years professional research experience and completion of University RATS Clinical Certification within one year of hire required.
Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills also required.
Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; and the ability to function independently.
Departments may require IRB CITI Course or IATA DGR training within a specified timeframe.
Departments may prefer a nursing degree for this position, which requires the incumbent to have two years related experience and possess a nationally recognized research compliance certification.
Position is patient-sensitive and must fulfill all associated requirements. All patient-sensitive employees must be immunized according to CDC standards and hospital policy (limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations).
Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.
Preferences
Master’s degree in a health science field.
Credentialing as an Association of Clinical Research Professionals (ACRP) Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Associates (SOCRA) Certified Clinical Research Professional (CCRP).
Special Instructions Requisition Number: PRN43953B
Full Time or Part Time?: Full Time
Work Schedule Summary
Department: 00917 – Vascular Surgery Development
Location: Campus
Pay Rate Range: $39,300 to $72,700
Close Date: 4/6/2026
Open Until Filled
To apply, visit
https://utah.peopleadmin.com/postings/194544
Equal Opportunity Employer University of Utah is an equal opportunity employer and welcomes diversity in the workplace. Applications will be considered in accordance with all applicable laws and regulations.
#J-18808-Ljbffr