Clinical Research Program Manager

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 Clinical Research Program Manager at The Shriners Hospital for Children will oversee and manage all aspects of clinical research programs, ensuring compliance with ethical guidelines, regulatory requirements, and institutional policies. This role involves strategic planning, operational execution, and the overall success of research initiatives aimed at improving pediatric care. Key Responsibilities Reporting to the Hospital Administrator and Research Programs Office at SHC International Headquarters, the CRPM provides support and leadership in accordance with SHC’s policies and procedures, SHC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. The CRPM 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. Overall, the CRPM is the site’s primary liaison among research participants, local study staff, the local investigator(s) and study sponsor(s). This position’s main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards. This position will provide management for the day-to-day operations of the clinical research program, ensure competent and standardized staff practices, and coordinate strategies to enhance interdisciplinary communication and collaboration. Required Qualifications Bachelors or master’s in clinical research, science or other healthcare related field preferred. Without a degree, 5 or more years of specific job-related experience in the administration of clinical research is required. Three years’ Clinical research experience, e.g. experience with site management, study management, IRB’s and federalregulations regarding clinical research compliance Preferred Qualifications Certified Clinical Research Coordinator Experience in the coordinationof intergroup or multi-site clinical studies Supervisory or management experience Compensation is determined based on years of relevant experience and departmental equity. #J-18808-Ljbffr