Duke Nurses are transforming the future of patient care. Guided by our mission, vision and values, we are committed to excellence. We are leaders, innovators, and educators. We are passionate about what we do. Duke University Health System Nursing is committed to quality care of our patients, their family members, and the community through excellence in leadership, practice, innovation, and education.
Coordinate DOCR’s portion of the Clinical Research Institutional Approval process. Review study documents to complete required start-up build in OnCore and meet with study teams to review the billing grid prior to the study orders and Beacon builds for Maestro Care. Collaborate with teams internal and external to DOCR to assess study readiness prior to go-live. Provide clinical guidance and training to Clinical Research Analysts regarding protocol interpretation and billing grid creation.
Post : CLINICAL RESEARCH ANALYST
Job Description
- Help with oversight of build assignment and metrics for research order sets and Beacon research treatment plans. Maintain REDCap database for tracking build and responsible for the DOCR Support Service Now queue.
- Review amendment and correction requests received through Service Now and DOCR-Startup, and coordinate with PRMO and the Research Maestro Care build team to make the appropriate changes in OnCore and Maestro Care (if applicable).
- Field questions from the research community about OnCore, Maestro Care and the DOCR review process.
- Review new studies in the DOCR approval queue in eIRB and OnCore (when in production). Assess and studies for operational needs (OnCore, Maestro Care builds) and coordinates the multi office work.
- Serve as a liaison with the PRMOClinical Trials Billing Office, identifying best practices and overseeing resolution of complex research billing issues.
- Collaborate with teams inside and outside of DOCR to assess study readiness to go-live.
- Identify studies requiring additional Maestro Care workflow/Study Planning support and refer these teams to the appropriate support resources.
- Provide guidance and training to Clinical Research Analysts regarding protocol interpretation and billing grid creation.
- Draft the majority of research billing grids for pediatric oncology studies.
Candidate Profile
Work requires graduation from an accredited degree program in a clinical field such as a Registered Nurse (RN), Physician's Assistant (PA) or Pharmacist plus two years of healthcare experience, or one of the following equivalents:
• Completion of an allied health degree (e.g., Respiratory Therapy, Ra-diologic Technology, Licensed Practical Nurse) or Associates degree in Clinical Trials Research related curriculum plus a minimum of five years clinical and/or research experience; or
• Completion of a bachelor's degree in a field related to health science and a minimum of three clinical and/or research experience.
Experience:
None required beyond that described above OR AN EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE Preferred: At least 2 of the years of clinical experience will include Super User-level usage of Epic software.
Additional Information
Experience : 2 years
Qualification : Nurse (RN), Physician's Assistant (PA) or Pharmacist
Location : Durham, NC
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : CR
Req ID : 401404790
See All US Jobs M.Sc Alerts M.Pharm Alerts
See All Other Jobs in our Database
.png)
