Nephrology Clinical Research Study Coordinator

University of Utah Health Research; Salt Lake City (UT); On-site; USD 32,000 - 66,000; Full time

Job summary

University of Utah Health Research is seeking a PS Study Coordinator to coordinate technical and administrative aspects of a clinical study under the Principal Investigator, ensuring protocol integrity and achievement of study objectives.

The role requires a Bachelor’s degree in a related field, IRB CITI certification within six months, strong communication skills, and diligence in maintaining regulatory documents. The position is full-time and based on the Salt Lake City campus.

Qualifications

• Bachelor’s degree in a related field is required or equivalent (one year of education can substitute for two years of related work experience).
• IRB CITI Course in the Protection of Human Research Subjects within six months of hire.
• Must be able to demonstrate the potential to perform essential functions of the job.

Responsibilities

• Assesses protocol for clarity and subject safety; reviews inclusion/exclusion criteria with PI and sponsor.
• Attends Investigator and staff meetings; advises the team on specific study assignments and timelines.
• Explains and documents informed consent, medical history and demographics; maintains source data and subject logs.
• Coordinates visit length and related facility/equipment availability.
• Reports adverse events and notifies IRB and sponsor as required.
• Documents protocol deviations and reconciles test article accountability at closeout.
• Prepares summary reports for sponsors and relays CRFs to sponsor.
• Assists with budget negotiation and payment terms.
• Maintains documents per FDA guidelines.

Skills

Effective communication

IRB CITI Course

Education

Bachelor’s degree in a related field

Job description

University of Utah Health Research is seeking a PS Study Coordinator to coordinate technical and administrative aspects of a clinical study under the Principal Investigator, ensuring protocol integrity and achievement of study objectives.

The role requires a Bachelor’s degree in a related field, IRB CITI certification within six months, strong communication skills, and diligence in maintaining regulatory documents. The position is full-time and based on the Salt Lake City campus.