Pediatric Clinical Research Coordinator II — Data

150 Shriners Hospitals for Children; United States; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Tuition assistance

Retirement matching

Job summary

Shriners Children’s in the United States seeks a Clinical Research Coordinator, Level 2 (CRC2) to oversee retrospective core activities, ensure compliance with GCP and regulations, and support data collection and study management across SHC sites.

You will collaborate with investigators, the Retrospective Core team, and sponsor representatives, maintain regulatory knowledge, contribute to protocol reviews, and help prepare abstracts and manuscripts while upholding patient safety and ethics.

Qualifications

• 3 years of clinical research experience, e.g. site management, study management, IRBs, and federal regulations.
• Bachelor's Degree in clinical research, science or other healthcare related field - or 5 years of specific job-related experience in the administration of clinical research.

Responsibilities

• Maintains a contemporary knowledge of clinical research regulatory requirements.
• Supports the investigators’ development of SHC investigator-initiated research protocols via the Retrospective Core.
• Supports the implementation of approved research protocols.
• Ensures studies are conducted in compliance with the approved protocol, Good Clinical Practice (GCP) guidelines, applicable regulatory requirements, SHC policies and standards.
• Coordinates the collection and management of data throughout a clinical study.

Skills

Regulatory compliance

IRB coordination

Data management

Education

Bachelor's Degree in clinical research, science or related field

5 years of related experience in clinical research

CCRP or CCRC certification

Tools

Python

SQL

Job description

Shriners Children’s in the United States seeks a Clinical Research Coordinator, Level 2 (CRC2) to oversee retrospective core activities, ensure compliance with GCP and regulations, and support data collection and study management across SHC sites.

You will collaborate with investigators, the Retrospective Core team, and sponsor representatives, maintain regulatory knowledge, contribute to protocol reviews, and help prepare abstracts and manuscripts while upholding patient safety and ethics.