Children's National Hospital - Washington, DC
posted 7 months ago
About the position
The Research Nurse Coordinator (RNC) at the Brain Tumor Institute plays a pivotal role in managing and coordinating clinical research projects. This position requires a high level of independence and expertise, as the RNC operates with minimal supervision while adhering to Good Clinical Practice (GCP) guidelines. The RNC is expected to possess a deep understanding of the clinical trials and grants process, as well as the federal and institutional regulations that govern clinical research, including those from JCAHO, FDA, GCP, OHRP, IRB, and NIH/NCRR. This role is not only about managing research protocols but also about ensuring the quality of care and facilitating collaboration among multidisciplinary teams to meet the complex needs associated with research processes. In addition to coordinating research projects, the RNC is responsible for meticulous documentation of all research-related procedures and outcomes. This includes continuous review of research processes and providing constructive feedback to the principal investigator, research coordinators, and other team members. The RNC also plays a crucial role in preparing Institutional Review Board (IRB) applications for clinical research proposals, ensuring that all nursing practices align with legal scopes, national standards, and institutional policies. The position emphasizes the importance of building relationships within the community to enhance the health and well-being of the population served. The RNC is expected to demonstrate strong clinical, organizational, and communication skills, acting as a resource for other professionals and setting standards for research quality. The role requires a commitment to professional development and participation in community activities, reflecting the organization's dedication to diversity and integrity in all practices.
Responsibilities
- Coordinate and manage clinical research projects in compliance with federal and institutional regulations.
- Maintain confidentiality of research data and ensure responsible conduct of research.
- Perform clinical assessments and integrate patient data to anticipate problems related to research protocols.
- Facilitate effective communication among research team members, patients, and families.
- Design and evaluate educational materials related to research protocols for staff and patients.
- Ensure informed consent is obtained from research subjects prior to participation.
- Promote safety and quality in research practices by validating information and addressing uncertainties.
- Participate in shared leadership and contribute to the organization's MAGNET Journey.
Requirements
- Minimum of 5 years of clinical research nursing coordinating NIH and industry-sponsored clinical trials.
- Completion of all Human Subject Research Courses (5 years required).
- At least 3 years of recent clinical nursing experience in an acute care setting.
- Meticulous attention to detail and strong organizational skills.
- Proficient computer skills, including familiarity with MS Word and MS Office.
Nice-to-haves
- Experience with pediatric clinical research.
- Knowledge of additional regulatory requirements for clinical trials.
- Familiarity with electronic health record systems.
Benefits
- Comprehensive health insurance coverage.
- 401k retirement savings plan with employer matching.
- Paid time off and holidays.
- Professional development opportunities and continuing education support.
