Clinical Study Coordinator: Patient-Centric Trials & Compliance

University of Utah; Salt Lake City (UT); On-site; USD 35,000 - 40,000; Full time

Job summary

University of Utah is seeking Clinical Study Coordinators to support the Neuroimmunology department on campus. This entry‑level role involves coordinating logistical and administrative aspects of clinical trials, assisting with participant recruitment, consent, documentation, and monitoring safety through study visits and adverse events tracking.

Requires a bachelor’s (or equivalent) with up to 2 years of related experience or a master’s (or equivalent).

Qualifications

• Bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree.
• Equivalency statements allow substitution of education for experience.
• Entry-level position in General Professional track.

Responsibilities

• Coordinate logistical and administrative aspects of clinical trials and studies.
• Assist with participant recruitment, consent processes, and documentation management.
• Coordinate study visits, monitor adverse events, and maintain accurate records for successful outcomes.

Skills

Bachelor

Clinical research

Regulatory compliance

Consent processes

Education

Bachelor's degree or equivalent

Master's degree or equivalent

Job description

University of Utah is seeking Clinical Study Coordinators to support the Neuroimmunology department on campus. This entry‑level role involves coordinating logistical and administrative aspects of clinical trials, assisting with participant recruitment, consent, documentation, and monitoring safety through study visits and adverse events tracking.

Requires a bachelor’s (or equivalent) with up to 2 years of related experience or a master’s (or equivalent).