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SalaryCompany Overview:
The Clinical Research Associate/Analyst (CRA) is a specialized, independent research professional who supports the Vice President, Research and the Corporate Director of Clinical Research with managing and maintaining system-wide Clinical Research operations, staff education, and compliance. This position’s responsibilities are to facilitate appropriate and ethical Clinical Research activities in accordance with the protocol, SHC’s policies and procedures, SHC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines. Additionally, the CRA is responsible for creating, implementing, maintaining, and overseeing the operational aspects of our organization’s research systems. This includes the Epic EMR, the CTMS (OnCore) and other supplemental systems. This role as an application liaison/coordinator primarily facilitates the use of the Epic application and its functionality for research-related activities.
Responsibilities:
Experience Preferred:
Education Required/Preferred:
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Shriners Children’s is a family 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 defines us as leaders in pediatric specialty care for our children and their families.
Job Overview:Shriners Children's is the premier pediatric burn, orthopaedic, spinal cord injury, cleft lip and palate, and pediatric subspecialties medical center. We have an opportunity for a Clinical Research Associate/Analyst reporting into our Corporate Headquarters location.
The Clinical Research Associate/Analyst (CRA) is a specialized, independent research professional who supports the Vice President, Research and the Corporate Director of Clinical Research with managing and maintaining system-wide Clinical Research operations, staff education, and compliance. This position’s responsibilities are to facilitate appropriate and ethical Clinical Research activities in accordance with the protocol, SHC’s policies and procedures, SHC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines. Additionally, the CRA is responsible for creating, implementing, maintaining, and overseeing the operational aspects of our organization’s research systems. This includes the Epic EMR, the CTMS (OnCore) and other supplemental systems. This role as an application liaison/coordinator primarily facilitates the use of the Epic application and its functionality for research-related activities.
Responsibilities:
Responsibilities include Clinical Research Operations; Compliance including monitorint of study specific essential documents, investigator/study personnel qualifications, and data safeguards to ensure research is being conducted; and Education including providing education and support to investigators and research staff.
Qualifications:Experience Required:
- 3 years of Clinical Research experience required, including site management, study management, IRB's, and federal regulations regarding Clinical Research compliance
- MS Office proficiency (Word, Excel, PowerPoint) required
- Experience with regulation and guidance(s) related to Clinical Research required
Experience Preferred:
- Coordination of intergroup or multi-site clinical studies preferred
Education Required/Preferred:
- High School/GED required
- Bachelor's Degree in Clinical Research, Science or other Healthcare related field with 3 years of job-specific experience required -OR- 5 years of job-specific experience in lieu of a Bachelor's Degree required
- CCRP or CCRC certification preferred
