Clinical Research Study Coordinator

University of Utah Health Research; Salt Lake City (UT); On-site; USD 32,000 - 48,000; Full time

Job summary

University of Utah Health seeks a PS Study Coordinator to coordinate clinical research studies in the Neurosurgery department. The role supports the Principal Investigator in implementing protocols and ensuring study integrity in a 40-hour work week.

Responsibilities include consent, data collection, AE reporting, CRF management, and regulatory document maintenance; strong communication and adherence to FDA/IRB guidelines are essential.

Qualifications

• Bachelor’s degree in a related field is required or equivalency.
• IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire.
• Vaccination requirements must be fulfilled or exemption approved.

Responsibilities

• Coordinate technical and administrative details for clinical/research studies.
• Assist PI in achieving study integrity and objectives.
• Explain and obtain informed consent; document demographics and history.

Skills

Communication skills

Education

Bachelor’s degree in a related field

IRB CITI Course in Protection of Human Research subjects

Job description

University of Utah Health seeks a PS Study Coordinator to coordinate clinical research studies in the Neurosurgery department. The role supports the Principal Investigator in implementing protocols and ensuring study integrity in a 40-hour work week.

Responsibilities include consent, data collection, AE reporting, CRF management, and regulatory document maintenance; strong communication and adherence to FDA/IRB guidelines are essential.