Coord II: Clin Research, CR

Shriners Children's; Philadelphia (Philadelphia County); On-site; USD 55,000 - 75,000; Full time

Job summary

Shriners Children's in the United States seeks a Clinical Research Coordinator to support pediatric studies, ensuring compliance with protocols, regulatory requirements, and ethical guidelines.

You will assist with patient recruitment, data collection, study documentation, and coordination with investigators, IRBs, and sponsors to report results. The role emphasizes Good Clinical Practices and collaborative teamwork within a pediatric hospital setting.

Qualifications

• Requires a Bachelor's degree or higher with 5+ years in clinical research administration.
• 3+ years of clinical research experience including site management and IRB attention.
• CCR or CCRC certification preferred.

Responsibilities

• Maintain current knowledge of clinical research regulatory requirements.
• Track study, investigator, IRB information, recruitment activity and budgeting.
• Collaborate with investigators, sponsors and regulatory agencies to report results.
• Coordinate data collection, analysis and dissemination of study results.
• Safeguard participants and ensure adherence to Good Clinical Practices.
• Support site research programs through timely communication and teamwork.

Skills

Clinical research coordination

IRB management

Regulatory compliance

Data collection

Study coordination

Education

Bachelor's degree in clinical research

Master's in clinical research

CCR/CCRC certification preferred

Job description

Company OverviewShriners 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 DescriptionJob SummaryCoordinates and supports clinical research studies, ensuring compliance with protocols, regulatory requirements, and ethical guidelines. This role involves assisting with patient recruitment, data collection, and maintaining accurate research documentation within a pediatric hospital setting.Key ResponsibilitiesMaintains a contemporary knowledge of clinical research regulatory requirements. Has a working knowledge of the complex clinical research process, from protocol development to implementationResponsible for tracking all aspects of projects including all study, investigator and Institutional Review Board (IRB) information, patient recruitment activity, and financial management Works closely with investigators, research leadership, study sponsor and regulatory agencies to conduct and report the results of clinical researchCoordinates the collection, statistical analysis and dissemination of data results throughout a clinical study. Evaluates protocols under consideration for feasibility, including the process for data collection, entry, storage and reportingSafeguards all participants involved in a research study supported and approved by Shriners Children'sFacilitates the local site’s research programs and projects through collaborative, timely communications and teamworkProvides expertise consultation and mentorship to site staff, residents, students, and volunteers with respect to research processes, Good Clinical Practices, and regulations governing clinical research. Interacts with other departments in a professional and timely manner to facilitate research coordination.Required QualificationsWithout a Bachelor's degree, 5 or more years of specific job-related experience in the administration of clinical research3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliancePreferred QualificationsBachelor's Clinical Research, science or other healthcare related fieldMaster's Clinical Research, science or other healthcare related fieldExperience in the coordination of intergroup or multi-site clinical studiesCCRP or CCRC certificationCompensation is determined based on years of relevant experience and departmental equity.