PS Clinical Research Coord

University of Utah; Salt Lake City (UT); On-site; USD 39,000 - 69,000; Full time

Job summary

The Department of Pediatric Cardiology at a leading university seeks a Clinical Research Coordinator to support research studies. Responsibilities include managing IRB submissions, ensuring compliance, and coordinating with research staff and patients. This full-time role offers competitive benefits and a supportive work environment.

Benefits

Excellent health care coverage

14.2% retirement contributions

Generous paid leave

50% tuition reduction

Flex spending accounts

Free transit on UTA services

Employee discounts

Professional development opportunities

Qualifications

• Two years of research experience required.
• Completion of University RATS Clinical Certification within one year of hire.

Responsibilities

• Manage IRB submissions, renewals, and regulatory documents.
• Coordinate with research staff and participants, including recruitment.
• Monitor budgets and research charges.

Skills

Communication

Organization

Software skills

Education

Bachelor’s degree in health sciences

Job description

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Job Summary

The Department of Pediatric Cardiology at the University of Utah, School of Medicine, has an immediate opening for a Clinical Research Coordinator to support Principal Investigators in the Division of Pediatric Cardiology. The role involves coordinating research studies, ensuring compliance with guidelines, and managing tasks such as IRB submissions, patient interfacing, consent acquisition, data supervision, and entry.

Benefits

• Excellent health care coverage at affordable rates
• 14.2% retirement contributions that vest immediately
• Generous paid leave and 11 holidays per year
• 50% tuition reduction for employees and dependents
• Flex spending accounts and free transit on UTA services
• Employee discounts and professional development opportunities

Responsibilities

1. Manage IRB submissions, renewals, and regulatory documents.
2. Ensure protocol compliance and oversee documentation and reporting.
3. Monitor budgets and research charges.
4. Coordinate with research staff and participants, including recruitment, scheduling, and consent.
5. Track data, recognize adverse events, and prepare for site visits.
6. Maintain regulatory documents and develop study materials.
7. Participate in ongoing training and coordinate with physicians and research teams.

Minimum Qualifications

Bachelor’s degree in health sciences or related field, two years of research experience, and completion of University RATS Clinical Certification within one year of hire. Knowledge of GCP, FDA, HIPAA, IRB regulations, and independent functioning are preferred.

Preferences

• Registered nurse or related clinical background.
• Experience in pediatrics or cardiovascular research.
• Certifications such as CCRC or CCRP.
• Strong organizational, communication, and software skills.

Additional Information

This is a full-time position, working 40 hours per week, Monday through Friday, with some flexibility. The pay range is $39,300-$68,349. Application details and further info are available at the application link.