Clinical Research Coordinator
About The Position
The Clinical Research Coordinator, Level 1 (CRC I) supports oversight and compliance for system-wide and local Shriners Children’s clinical research activities. The role reports to the Clinical Research Program Manager or, where applicable, the local Hospital Administrator or Clinic Director, and collaborates with the Research Programs Office at SHC International Headquarters. Work follows SHC policies and procedures, hospital regulations, the Code of Federal Regulations, and Good Clinical Practice (GCP) guidelines when applicable. The CRC works with investigators, research staff, and clinical teams to ethically recruit and consent pediatric research participants and to collect, manage, and safeguard research data. The coordinator serves as a liaison among participants, investigators, sponsors, and regulatory bodies, supporting proper study conduct, participant safety, and the quality and integrity of study data.
Requirements
- At least 1 year of relevant research experience, such as study coordination, site management, regulatory submissions, or clinical data management.
Nice To Haves
- Bachelor’s degree in Clinical Research, Life Sciences, Public Health, or another healthcare-related field.
- Working knowledge of clinical research regulations and guidance, such as GCP, FDA regulations, and IRB requirements.
- Experience coordinating intergroup or multi-site clinical studies.
- CCRP or CCRC certification.
Responsibilities
- Support implementation and conduct of approved research protocols in compliance with protocols, GCP, applicable regulations, and SHC policies and standards.
- Perform study-specific research activities and interventions within the bounds of professional licensure and training.
- Assist with participant recruitment, screening, informed consent and assent, scheduling, and study-visit coordination.
- Coordinate the collection and documentation of research data.
- Maintain regulatory documentation and study records in accordance with institutional policies and sponsor requirements.
- Support communication and coordination among investigators, sponsors, monitors, and institutional departments involved in research activities.
- Assist investigators with developing and submitting investigator-initiated research protocols and related regulatory documentation.
- Contribute to study progress reports, monitoring visits, audits, and preparation of study results or presentations when applicable.
- Complete appropriate training and education to safely perform study-related procedures and protocol requirements.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
