Clinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027)
Company Overview
Shriners Children’s is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, 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 define us as leaders in pediatric specialty care for our children and their families.
With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family’s ability to pay or insurance status. Please click here to learn more about our locations.
Job Description
The Clinical Research Coordinator I is a research professional who ensures oversight and compliance of both system-wide and local clinical research activities. Works collaboratively with research personnel to ethically recruit and consent pediatric subjects and to appropriately collect and safeguard data. Overall, the Clinical Research Coordinator is the site's primary liaison among research participants, the local investigator(s) and study sponsors.
Key Responsibilities:
Ensure proper study conduct, subject safety, and the quality of data and data safeguards
Timely data collection
Ensure accurate data entry into secure research databases
Verify data accuracy through internal quality control measures
Provides timely responses to data queries
Confirms appropriate training and education are in place to safely perform study protocols.
Effectively provides information about the use of investigational products to patients.
Other duties as assigned.
The Clinical Research Coordinator I position is open to current medical students enrolled at the University of South Carolina School of Medicine Greenville. This is a Temporary Position tentatively running from July 20, 2026-July 20, 2027.
Required Qualifications:
Bachelor's degree in clinical research, science or other healthcare field
At least one (1) year of relevant research experience, e.g. site management, study management, research regulatory experience, data collection, compliance or other applicable experience
Working knowledge of the clinical research process
Knowledge of ethical standards for research and a commitment to protect all participants
Preferred Qualifications:
Master's degree in related field
Certification: CCRP or CCRC
Bilingual (English/Spanish)