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Study Coordinator (15240B)

#16047
University of Utah, Division of Human Resources

Details:

  • Category: Off-Campus
  • Position Type: Full-Time (Career)
  • Posted on: September 11, 2017
  • Open until: Sun, December 10, 2017 expired
  • Wage: $31,600 to $47,000/year
  • Location: Salt Lake City, Utah, UT

Description:

A Study Coordinator is needed for the Diagnostic Neuroimaging Laboratory. The Study Coordinator will coordinate technical and administrative details involved in Diagnostic Neuroimaging studies; specifically, studies concerning veteran mental health at the Salt Lake City VA and the University Neuropsychiatric Institute. The Study Coordinator will assist the Principal Investigator in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures.

University of Utah Job ID# PRN15240B, Diagnostic Neuroimaging

COMPENSATION: $31,600 to $47,000/year. Strong benefit package including generous leave accrual, retirement and health plan options.

WORK SCHEDULE: Full-time, 40 hour/week, days.

RESPONSIBILITIES: 1. Assesses protocol for clarity and subject safety, reviews inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator and sponsor. 2. Attends and participates in Investigator and staff meetings. Advises team regarding specific study assignments and timelines. 3. Explains and obtains informed consent, medical history and demographics; documents in source file and maintains with historical data, status reports, progress notes, and subject log to help ensure subject safety. 4. Determines length of visits and coordinates related facility and equipment availability. 5. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. 6. Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor. 7. Completes, audits, corrects CRFs, relays CRFs to sponsor. 8. Assists with negotiating contract budget and payment terms. 9. Maintains documents as required by FDA guidelines. 10. May maintain contact with IRB and prepare and submit IRB documents. 11. May ensure proper collection, processing and shipment of specimens. 12. May perform functions required of the Clinical Research Assistant as necessary.

Qualifications:

QUALIFICATIONS: Bachelor’s degree in a related field, or equivalency required. IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire and demonstrated human relations and effective communication skills are also required.

Application Instructions:

PLEASE APPLY ONLINE THROUGH THE UNIVERSITY OF UTAH SYSTEM TO BE CONSIDERED FOR THIS JOB: http://utah.peopleadmin.com/postings/68978

EQUAL EMPLOYMENT OPPORTUNITY The University of Utah is an Affirmative Action/Equal Opportunity employer. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities. Please contact the Office of Equal Opportunity and Affirmative Action, 201 S. Presidents Cr., Rm 135, (801) 581-8365 (V/TDD), for further information or to request an accommodation. The University of Utah is committed to diversity in its workforce. Women and minorities are encouraged to apply.


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