Coordinator II, Clinical Research

Shriners Children's • Salt Lake City, UT

26d

About The Position

The Clinical Research Coordinator II (CRC) is a specialized, independent research professional responsible for oversight and compliance of system-wide and local SHC clinical research activities. The CRC supports research in accordance with SHC policies and procedures, hospital regulations, the Code of Federal Regulations, and Good Clinical Practice guidelines, when applicable.

Working closely with the Chief of Staff, SHC scientific and medical staff, and other research personnel, the CRC ethically recruits and consents pediatric research participants and appropriately collects and safeguards data. The CRC serves as the site’s primary liaison among research participants, local investigators, and study sponsors. The role focuses on proper study conduct, participant safety, data quality, and data safeguards.

Requirements

• At least 3 years of clinical research experience, such as experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance.
• If the candidate does not have a bachelor's degree, at least 5 years of specific job-related experience in clinical research administration.

Nice To Haves

• Bachelor’s degree in clinical research, science, or another healthcare-related field.
• Master’s degree in clinical research, science, or another healthcare-related field.
• Experience coordinating intergroup or multi-site clinical studies.
• CCRP or CCRC certification.

Responsibilities

• Maintain current knowledge of clinical research regulatory requirements and working knowledge of the clinical research process, from protocol development through implementation.
• Track all aspects of projects, including study, investigator, and IRB information; patient recruitment activity; and financial management.
• Work with investigators, research leadership, study sponsors, and regulatory agencies to conduct clinical research and report its results.
• Coordinate the collection, statistical analysis, and dissemination of data results throughout a clinical study.
• Evaluate protocols for feasibility, including processes for data collection, entry, storage, and reporting.
• Safeguard participants in research studies supported and approved by Shriners Children’s.
• Facilitate local research programs and projects through collaborative, timely communication and teamwork.
• Provide consultation and mentorship to site staff, residents, students, and volunteers on research processes, Good Clinical Practices, and clinical research regulations.
• Interact professionally and promptly with other departments to facilitate research coordination.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed