Clinical Research Nurse Coordinator, Duke Cance Institute
Duke UniversityAbout the role
Clinical Research Nurse Coordinator, Duke Cance Institute
Oncology Clinical Research Unit [CRU]
Cancer control population Science Clinical Research Program (CCPS)
Position Description, 1
Occupational Summary
Provide leadership in the development, implementation and management of research for the Duke Cancer Institute’s (DCI) Cancer Control Population Science (CCPS) Clinical Research Program; the Oncology Clinical Research Unit (CRU) provides research oversight. Serve as the primary liaison throughout the institution for assigned projects. Responsible for managing projects through the entire lifecycle, from concept to initiation to closeout: responsible for project results including costs and reporting.
Work Preformed
Program, Project and Study Management – 50% Effort
Work closely with the Principal Investigator (PI) and research team on goals, study feasibility, design, protocols, resources, and recruitment and retention strategies. Evaluate plans, processes and results to make recommendations for improvement; develop and implement solutions. Contribute expertise in research design to develop protocol and research proposals. Evaluate and include cultural diversity and competency in study design and conduct.
Assist with budget development; monitor and adhere to the established budget.
Participate in, and provide oversight, including communication, for IRB submissions and documentation, regulatory and safety reporting, and adverse events. Coordinate Duke core services such as Investigational Drug Service (IDS) and Biobank. Be familiar with intellectual property rights, inventions patents, and technologies. Understand regulations related to investigational products with sponsors. Manage agreements such as Material Transfer and Investigational New Drug Applications.
Assist with the development, selection, and implementation of data capture methods and protocol-specific systems and documents. Oversee the design of data forms such as; electronic case reporting forms (ECRF), electronic data capture (EDC), data flow, queries, quality assurance, and data security. Develop safety and security documents such as research data storage plans (RDSP), conflict of interest (COI), and data safety management plans (DSMP).
Science – 10% Effort
Collaborate with stakeholders (statistical, operational, etc.) to ensure adequate design, implementation and testing of study aims. Develop research proposals or protocols with little assistance. Summarize study results.
Contribute significant writing and editing to grant and funding proposals and the development of investigator-initiated studies. Read and analyze literature to assist with manuscripts. Keep current on scientific advances.
Communication – 10% Effort
Collaborate, and communicate with PI and study personnel as required. Communicate concerns clearly in a professional manner. Respond timely to emails, phone calls and questions. Escalate issues to others as appropriate.
Leadership – 15% Effort
Serve as an expert resource for colleagues and teammates. Assist colleagues in identifying efficiencies and improving process. Support colleagues in their project work; encourage completion. Actively network.
Provide leadership within the team. Mentor staff. Prepare for, lead and participate in team meetings, committees, task forces and ad hoc groups.
Supervisory – 10% Effort
Lead, supervise and manage staff including coaching, mentoring, time-off, annual performance review, performance management, career development, training, hiring and termination. Collaborate closely with DCI HR in all aspects of staff management.
Create a team culture that fosters open communication, motivates and ret
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