Clinical Research Program Manager

Shriners Hospitals for Children • Sacramento, CA

4d • Onsite

About The Position

The Clinical Research Program Manager (CRPM) is a specialized, independent research professional responsible for the operational management and oversight of all local Shriners Children’s (SC) clinical research activities. Reporting to the Hospital Administrator and the Research Programs Office at SHC International Headquarters, the CRPM provides support and leadership in accordance with SC's policies and procedures, SC's regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, where applicable. The CRPM collaborates closely with the Chief of Staff, SC scientific and medical staff, and other research personnel to ethically recruit and consent SC's vulnerable pediatric subjects and to appropriately collect and safeguard data. This position serves as the site's primary liaison among research participants, local study staff, the local investigator(s), and study sponsor(s). The main responsibilities of this position are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards. This position will manage 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.

Requirements

• Bachelors in Clinical Research or if no degree, 5 or more years of specific job-related experience in the administration of clinical research is required.
• 3 years clinical research experience, e.g. experience with site management, study management, IRB's and federal regulations regarding clinical research compliance

Nice To Haves

• Certified Clinical Research Coordinator
• Master's degree in clinical research

Responsibilities

• Accountable for the site's research activities
• Work effectively with SHC leadership to ensure the research mission is upheld
• Coordinate with the Department of Research Programs regarding clinical activities
• Provide expertise, consultation and mentorship to site staff
• Directs education and training to clinical research staff
• Coordinates resources and services to successfully implement and monitor progress of clinical research
• Supports the implementation of approved research protocols
• Responsible for tracking all aspects of projects including (but not limited to) Institutional Review Board (IRB) information, patient recruitment activity, and financial management
• Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level