Clinical Trials Coordinator - Regulatory & Data Specialist

Utah; Murray (UT); On-site; USD 55,000 - 75,000; Full time

Job summary

The University of Utah is seeking a Clinical Research Coordinator to coordinate day-to-day clinical trial activities in line with Good Clinical Practices (GCPs). The role involves managing study protocols, participant recruitment, and maintaining regulatory compliance.

Applicants are required to have a Bachelor’s degree in health sciences and at least two years of professional research experience. This position also entails patient-sensitive responsibilities and compliance with immunization standards.

Qualifications

• Bachelor’s degree in a health sciences or related field required.
• Two years of professional research experience is mandatory.
• Exceptional organizational skills and attention to detail are required.

Responsibilities

• Coordinate day-to-day clinical trial activities according to protocols.
• Conduct pre-study, site qualification, and monitoring activities.
• Recruit and enroll study participants and maintain data.

Skills

Organizational skills

Attention to detail

Effective communication

Knowledge of Good Clinical Practices

Education

Bachelor’s degree in health sciences or related field

Completion of University RATS Clinical Certification

Nursing degree (preferred)

Job description

The University of Utah is seeking a Clinical Research Coordinator to coordinate day-to-day clinical trial activities in line with Good Clinical Practices (GCPs). The role involves managing study protocols, participant recruitment, and maintaining regulatory compliance.

Applicants are required to have a Bachelor’s degree in health sciences and at least two years of professional research experience. This position also entails patient-sensitive responsibilities and compliance with immunization standards.