Clinical Research Coordinator II - Shriners Children's

Shriners Children’s is a family that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience defines us as leaders in pediatric specialty care for our children and their families.

Shriners Children's is the premier pediatric burn, orthopaedic, spinal cord injury, cleft lip and palate, and pediatric subspecialties medical center.  We have an opportunity for a Clinical Research Coordinator. 

The Clinical Research Coordinator is a research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities. Provides support in accordance with SHC’s policies and procedures, SHC’s hospital regulations, the Code of Federal Regulation and Good Clinical Practice guidelines, when applicable.  Works collaboratively with research personnel to ethically recruit and consent SHC’s vulnerable pediatric subjects and to appropriately collect and safeguard data.  Overall, the CRC is the site’s primary liaison among research participants, the local investigator(s) and study sponsor(s).  This position’s main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.  This may include, but is not limited to, subject recruitment and data/specimen collection of SHC’s system-wide projects. 

Education

Bachelors degree in clinical research, science or other healthcare related field preferred. Without a Bachelors degree, 5 or more years of specific job-related experience in the administration of clinical research is required.

Master’s degree in clinical research, science or other healthcare related field preferred

Certification/Licensure

Professional Licensure (e.g. nursing, PT, OT)

CCRP or CCRC certification preferred

Experience

Three or more years of clinical research experience required (site management, study management, IRBs, and federal regulations regarding clinical research compliance)

Other

Current full vaccination status required