Pediatric Retrospective Clinical Research Coordinator II

Shriners Children's; United States; A distancia; USD 70.000 - 95.000; Jornada completa

Descripción de la vacante

Shriners Children’s is seeking a Clinical Research Coordinator, Level 2, to oversee retrospective core studies and ensure compliant, high-quality data collection across SHC sites. You will work with the CRPM, investigators, and staff to support protocol development and data management while adhering to regulatory standards.

The role emphasizes safeguarding participant data, coordinating IRB submissions, and ensuring study integrity through timely data entry, verification, and reporting to

Formación

• 3 years of clinical research experience including site management and IRB oversight.
• Bachelor’s degree or 5 years of related experience in clinical research administration.
• Experience with federal regulations governing clinical research and GCP.

Responsabilidades

• Wields knowledge of regulatory requirements for clinical research and GRP in practice.
• Supports investigator-initiated protocols via the Retrospective Core.
• Assists with implementation of approved research protocols and data capture.
• Monitors study conduct to ensure protocol compliance and safety standards.
• Tracks study, investigator, IRB information; coordinates with Legal and Compliance.
• Coordinates data collection, storage, entry, and quality control for studies.
• Terminates data queries, resolves discrepancies, and supports data cleaning.
• Contributes to study results reporting, abstracts, and manuscripts as needed.

Conocimientos

Clinical research coordination

Regulatory knowledge

Attention to detail

Team collaboration

Educación

Bachelor’s Degree in clinical research, science or healthcare field

5 years of specific job-related experience in clinical research administration

Herramientas

Python

SQL

Data management systems

Descripción del empleo

Shriners Children’s is seeking a Clinical Research Coordinator, Level 2, to oversee retrospective core studies and ensure compliant, high-quality data collection across SHC sites. You will work with the CRPM, investigators, and staff to support protocol development and data management while adhering to regulatory standards.

The role emphasizes safeguarding participant data, coordinating IRB submissions, and ensuring study integrity through timely data entry, verification, and reporting to