Clinical Research Coordinator II
Listed on 2026-01-12
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Healthcare
Clinical Research -
Research/Development
Clinical Research
Clinical Research Coordinator II – Shriners Children’s
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 multidisciplinary education, and research with global impact. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care.
The Clinical Research Coordinator (CRC) is a specialized, independent research professional who ensures oversight and compliance of both system‑wide and local clinical research activities. Reporting to the Clinical Research Program Manager or local Hospital Administrator / Clinic Director, the CRC provides support in accordance with Shriners children’s policies and regulations, the Code of Federal Regulations, and Good Clinical Practice guidelines. The CRC works closely with the Chief of Staff, scientific and medical staff, and other research personnel to ethically recruit and consent vulnerable pediatric subjects and to appropriately collect and safeguard data.
The CRC is the site’s primary liaison among research participants, the local investigator(s) and study sponsor(s).
- Maintain contemporary knowledge of clinical research regulatory requirements and the complex clinical research process from protocol development to implementation.
- Track all aspects of projects including study, investigator and Institutional Review Board (IRB) information, patient recruitment activity, and financial management.
- Work closely with investigators, research leadership, study sponsors and regulatory agencies to conduct and report the results of clinical research.
- Coordinate the collection, statistical analysis and dissemination of data results throughout a clinical study; evaluate protocols under consideration for feasibility, including the process for data collection, entry, storage and reporting.
- Safeguard all participants involved in a research study supported and approved by Shriners Children’s.
- Facilitate the local site’s research programs and projects through collaborative, timely communications and teamwork.
- Provide expertise, consultation and mentorship to site staff, residents, students, and volunteers with respect to research processes, Good Clinical Practices, and regulations governing clinical research; interact with other departments professionally and timely to facilitate research coordination.
- Without a Bachelor's degree, 5 or more years of specific job‑related experience in the administration of clinical research.
- 3 or more years of clinical research experience, e.g., experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance.
- Bachelor’s degree in Clinical Research, science, or other healthcare related field.
- Master’s degree in Clinical Research, science, or other healthcare related field.
- Experience in coordinating intergroup or multi‑site clinical studies.
- CCRP or CCRC certification.
Mid‑Senior level
Employment typeFull‑time
Job functionResearch, Analyst, and Information Technology
IndustriesHospitals and Health Care
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