Pediatric Clinical Research Coordinator

Shriners Children's

Galveston (TX)

On-site

USD 60,000 - 76,000

Full time

7 days ago
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Job summary

Shriners Children’s in Texas is seeking a Clinical Research Coordinator, Level 1 (CRC I) to support oversight of system-wide and local research activities, under the Research Programs Office. You will collaborate with investigators, staff, and clinical teams to recruit and consent pediatric participants and safeguard study data.

The role emphasizes compliance with GCP, FDA regulations, IRB requirements, and SHC policies, with responsibilities spanning data collection, regulatory documentation,

Qualifications

  • 1+ year of relevant research experience (study coordination, site management, regulatory submissions, or data management).
  • Bachelor’s degree in Clinical Research, Life Sciences, Public Health, or related field preferred.
  • Knowledge of GCP, FDA regulations, IRB requirements encouraged.

Responsibilities

  • Supports implementation and conduct of approved protocols in compliance with GCP and SHC policies.
  • Assists with participant recruitment, consent, scheduling, and coordination of visits.
  • Coordinates collection and documentation of research data.
  • Maintains regulatory documentation and study records.
  • Supports communication between investigators, sponsors, monitors, and departments involved in research activities.
  • Contributes to study progress reports and audits.

Skills

Study coordination
Regulatory compliance
Participant recruitment

Education

Bachelor’s degree in Clinical Research, Life Sciences, Public Health, or related field
CCRP or CCRC certification

Job description

Shriners Children’s in Texas is seeking a Clinical Research Coordinator, Level 1 (CRC I) to support oversight of system-wide and local research activities, under the Research Programs Office. You will collaborate with investigators, staff, and clinical teams to recruit and consent pediatric participants and safeguard study data.

The role emphasizes compliance with GCP, FDA regulations, IRB requirements, and SHC policies, with responsibilities spanning data collection, regulatory documentation,

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