Shriners Children’s is an organization that respects, supports, and values each other. 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.

All employees are eligible for medical, dental and vision coverage on their first day! In addition, upon hire all employees are eligible for a 403(b) and Roth 403 (b) Retirement Saving Plan with matching contributions of up to 6% after one year of service. Employees in a FT or PT status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans. Additional benefits available to FT and PT employees include tuition reimbursement, home & auto, hospitalization, critical illness, pet insurance and much more! Coverage is available to employees and their qualified dependents in accordance with the plans. Benefits may vary based on state law.

The Clinical Research Coordinator, Level 2 (CRC2) is a specialized, independent research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities.  Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and Research Programs Office at SHC International Headquarters, the CRC 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.  The CRC 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 CRC is the sites primary liaison among research participants, the local investigators and study sponsors.  This position's main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.  We have an opportunity for a Clinical Research Coordinator II. in our Salt Lake Facility.

Schedule: Full-time FTE 1.0 (in-person)

Holidays: 9 observed holidays per year

• Maintains a contemporary knowledge of clinical research regulatory requirements.  Has a working knowledge of the complex clinical research process, from protocol development to implementation.
• Coordinates the collection, statistical analysis and dissemination of data results throughout a clinic study.  Evaluates protocols under consideration for feasibility, including the process for data collection, entry, storage and reporting.
• Safeguards all participants involved in a research study supported and approved by Shriners Children's.  Maintains patient safety and privacy throughout the study.
• Confirms appropriate training and education are in place to safely perform study protocols.  Adheres to and applies protocol eligibility criteria when recruiting patients.
• Demonstrates  clear understanding and an ethical and legally effective informed consent process. Effectively communicates with participants/families during the consent.
• Facilitates the local site's research programs and projects through collaborative, timely communications and teamwork.  Exhibits excellent communication and collaboration in all aspects of the research program within the site; between the site and the sponsor and with appropriate outside entities.
• Works effectively with SHC leadership to ensure the research mission is upheld.  Maintains scientific integrity, intellectual honesty, and excellence.

Note:  This is not an all-inclusive list of this job's responsibilities.  The incumbent may be required to perform other related duties and participate in special projects as assigned.

Education

• Bachelor's  Clinical Research, science or other health-care related field, Preferred
• Master’s  Clinical Research, science or other health-care related field, Preferred
• Without a Bachelor's degree, 5 or more years of specific job related experience in the administration of clinical research is required.

Experience

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

Certification and Licensures

• CCRP or CCRC certification, Preferred