Clinical Study Coordinator — Research & Protocol Lead

University of Utah; Salt Lake City (UT); On-site; USD 65,000 - 100,000; Full time

Job summary

University of Utah seeks a Clinical Study Coordinator to independently manage technical and administrative tasks for multiple trials. You will lead recruitment and consent, maintain thorough study documentation, and ensure protocol adherence for safety and integrity.

Responsibilities include auditing CRFs, negotiating budgets with minimal supervision, coordinating IRB submissions, and ensuring proper specimen handling and shipment in accordance with FDA guidelines.

Qualifications

• Requires a bachelor’s (or equivalency) + 8 years or a master’s (or equivalency) + 6 years of directly related work experience.

Responsibilities

• Independently coordinate technical and administrative details for multiple trials.
• Lead recruitment and consent processes, and maintain comprehensive and accurate study documentation.
• Audit and correct CRFs for completeness and accuracy, negotiate contract budgets and payment terms with minimal supervision, maintain contact with the IRB, and manage IRB document submissions.
• Ensure proper collection, processing, and shipment of specimens.

Skills

Coordination

Informed consent

Regulatory documentation

Budget negotiation

Education

Bachelor's Degree

Master's Degree

Job description

University of Utah seeks a Clinical Study Coordinator to independently manage technical and administrative tasks for multiple trials. You will lead recruitment and consent, maintain thorough study documentation, and ensure protocol adherence for safety and integrity.

Responsibilities include auditing CRFs, negotiating budgets with minimal supervision, coordinating IRB submissions, and ensuring proper specimen handling and shipment in accordance with FDA guidelines.