Pediatric Clinical Research Coordinator

Shriners Hospitals for Children; Galveston (TX); Presencial; USD 52.000 - 76.000; Jornada completa

Descripción de la vacante

Shriner's Hospitals for Children is seeking a Clinical Research Coordinator, Level 1, to support oversight and compliance of clinical research activities across SHC. The CRC I will collaborate with investigators, sponsors, and regulatory bodies to ensure ethical recruitment, consent, data collection, and study integrity.

Responsibilities include coordinating study visits, maintaining regulatory documents, and assisting with protocol submissions while adhering to GCP and applicable FDA

Formación

• 1+ year of relevant research experience (e.g., study coordination, regulatory submissions, or clinical data management).
• Understanding of GCP, FDA regulations, and IRB requirements is preferred.
• CCRP or CCRC certification is a plus.

Responsabilidades

• Supports implementation and conduct of approved research protocols in compliance with GCP and SHC policies.
• Assists with participant recruitment, screening, and informed consent/assent.
• Coordinates collection and documentation of research data and maintains regulatory documentation.
• Communicates with investigators, sponsors, monitors, and departments involved in research activities.
• Contributes to study progress reports, audits, and preparation of results or presentations.
• Ensures training is completed for study-related procedures and protocol requirements.

Conocimientos

Research coordination

Regulatory submissions

Clinical data management

Study coordination

Educación

Bachelor's degree in Clinical Research, Life Sciences, Public Health, or related field

Descripción del empleo

Shriner's Hospitals for Children is seeking a Clinical Research Coordinator, Level 1, to support oversight and compliance of clinical research activities across SHC. The CRC I will collaborate with investigators, sponsors, and regulatory bodies to ensure ethical recruitment, consent, data collection, and study integrity.

Responsibilities include coordinating study visits, maintaining regulatory documents, and assisting with protocol submissions while adhering to GCP and applicable FDA