Clinical Research Coordinator II
@ 150 Shriners Hospitals for ChildrenClinical Research Coordinator II
About the job
Shriners Children’s is a top-ranked pediatric healthcare organization with 20+ hospitals providing exceptional care, research, and education globally. The role focuses on supporting clinical studies, ensuring protocol adherence, data management, and participant interaction under supervision.
Requirements
- 3+ years clinical research experience
- Experience with IRBs and regulations
- Study management and data tracking
- Participant interaction knowledge
Qualifications
- Bachelor's degree in healthcare field
- Master’s degree preferred
- Good communication skills
- Detail-oriented and team player
Full job description
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.
CURRENT EMPLOYEES: Please log into Workday Click Here to apply internally through the "Jobs Hub"
Job Description
Job Summary
The Coordinator II, Clinical Research supports clinical research studies at Shriners Hospitals for Children, ensuring adherence to protocols, regulatory requirements, and ethical guidelines. This role involves assisting with study coordination, data management, and participant interaction under direct supervision.
Key Responsibilities
- Supports the implementation of approved research protocols
- Ensures studies are conducted in compliance with the approved protocol, Good Clinical Practice guidelines, applicable regulatory requirements, SHC policies and standards
- Responsible for tracking all aspects of projects including all study, investigator and IRB information, patient recruitment activity and financial management
- Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study
- Safeguards all participants involve din a research study support and approved by the organization
- Facilitates the local site's research programs and projects through collaborative, timely communication and teamwork
Required Qualifications
- 3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance is required
Preferred Qualifcations
- Bachelors degree in clinical research, science or other healthcare related field preferred
- Master’s degree in clinical research, science or other healthcare related field preferred