Coordinator II: Clinical Research

Company Overview

Shriners Children’s is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.

With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family’s ability to pay or insurance status. Please click here to learn more about our locations.

Job Description

Job Summary

The coordinator II: Clinical Research supports and assists in the conduct of clinical research studies, ensuring adherence to protocols, regulations, and ethical guidelines. This role involves managing study-related documentation, coordinating patient visits, and contributing to data collection and integrity.

Key Responsibilities

• Help ensure proper study conduct, subject safety, and the quality of data and data safeguard

• Provides support in accordance with SHC’s policies and procedures, SHC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable

• Works closely with the Chief of Staff, SHC scientific and medical staff and other research personnel to ethically recruit and consent SHC’s vulnerable pediatric subjects and to appropriately collect and safeguard data

Required Qualifications

• Bachelor's degree in clinical research, science or other healthcare field preferred, but without a Bachelor's degree, 5 or more years of specific job-related experience in the administration of clinical research is required

• 3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance

Preferred Qualifications

• Master's degree in clinical research, science or other healthcare field preferred

• CCRP or CCRC preferred

• Experience in the coordination of intergroup or multi-site clinical studies