Clinical Study Coordinators

This position is patient-sensitive and must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work. We protect our patients, coworkers and community by requiring all patient-sensitive employees to 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.

About the role

Coordinate technical and administrative aspects of clinical studies, supporting research goals and protocol implementation. Assist with participant recruitment, consent processes, documentation, logistics, adverse event monitoring, and budget negotiations. Ensures accuracy and compliance while managing specimen handling for successful study outcomes.

Responsibilities

• Helps with the logistical and administrative aspects of clinical trials and studies, ensuring adherence to protocols and regulatory requirements.
• Facilitate participant recruitment, consent processes, and documentation management.
• Coordinate study visits, monitor adverse events, and maintain accurate records for successful study outcomes.

Requirements

• Clinical Study Coordinator, I: Requires a bachelor's degree (or equivalency) with up to 2 years of directly related work experience or a master's degree (or equivalency).
• Clinical Study Coordinator, II: Requires a bachelor's degree (or equivalency) plus 4 years or a master's degree (or equivalency) plus 2 years of directly related work experience.

EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor's degree = 4 years of directly related work experience).

Pay

Expected pay range: $35,000 - $40,000

Department may hire at any of the following pay rates based on business need and budget: $22,475 to $51,559

Schedule

Full Time

Location

Campus (University of Utah)