Research Nurse I, RN, Vaccine Clinical Trials

In addition to the responsibilities listed below, this position is also responsible for developing a basic clinical research knowledge in general aspects of nursing practice; participating in the implementation of new protocols; administering research interventions; evaluating the patients response to therapy; reporting variances to the research team; integrating evidence-based practice into nursing practice and evaluating patient outcomes; providing nursing care and judgement of research activities within scope of practice; communicating the impact of the research process on patient care; supporting the adjustment of interventions based on findings; supporting collaborating with the interdisciplinary team on basic improvement activities related to promoting patient/participant safety, clinical quality and reducing risk; and supporting the implementation of quality improvement activities in the team or program of care level.

Pursues effective relationships with others by sharing information with coworkers and members. Listens to and addresses performance feedback. Pursues self-development; acknowledges strengths and weaknesses, and takes action. Adapts to and learns from change, challenges, and feedback. Responds to the needs of others to support a business outcome. Completes routine work assignments by following procedures and policies and using data, and resources with oversight and management. Collaborates with others to address business problems; escalates issues or risks as appropriate; communicates progress and information. Adheres to established priorities, deadlines, and expectations. Identifies and speaks up for improvement opportunities. Assists in budgeting and financing by: learning about the budgeting process. Assists with clinical research by: collecting data in clinical trials (e.g., recruiting human subjects, administering surveys and/experiments) with substantial guidance; developing a basic understanding of source data and the tools leveraged to analyze clinical data; developing a basic understanding of clinical trials, studies, and interventions at the site-level; following detailed instructions while contributing to the development of routine clinical research protocols and other processes of clinical trials; understanding study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for supporting or executing basic clinical trial activities (e.g., informed consent process, lab support and processing, pharmaceutical documentation data, sample processing, adverse event assessment process); and may be involved in supporting basic research lab operations(e.g., biological specimen collection, including patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens), with guidance. Learns about research compliance by: learning to document clinical trial applications and relevant data in compliance and consistency with all applicable federal, state, and local regulations and KP policies and procedures; learning the fundamentals of compliance and quality including issue identification and resolution; performing quality assurance checks/audits on compliance-monitoring/audit systems and documentation, escalating when necessary; learning to and performing data entry tasks with guidance from a supervisor to assist with risk-management; learning about and implementing the research protocols, procedures, and guidance to ensure confidentiality, privacy, and security of clinical research data with guidance; and leveraging basic research expertise to supplement the guidance provided to investigators and other key stakeholders to ensure compliance with IRB approved protocols and local and federal guidelines. Learns to maintain internal and external effective working relationships by: developing a basic knowledge about important research