Research Interventionist Nurse III (28 hours​/week Silverdale

Research Interventionist Nurse III (28 hours/week Silverdale)

Would you like to fill an important role on a CDC research study to see how well the flu vaccine works? This position lasts about 4-6 months during flu season and enrolls patients being seen at Urgent Care with a respiratory illness. We are hiring for 4 Kaiser Permanente Washington clinics.

The Research Interventionist Nurse will review EPIC schedules, screen, consent, administer a questionnaire and collect nose and throat swabs from participants.

The ideal candidate is self-motivated, enjoys people and working in a dynamic environment. Requires extreme attention to detail and ability to work well independently and as a part of a team. Experience recruiting participants in a clinical setting is a plus.

We welcome applicants that reflect the broad diversity and lived experiences in our communities.

In addition to the responsibilities listed below, this position is also responsible for leveraging foundational clinical, healthcare, and research knowledge to support research studies to advance evidence-based practices with limited guidance; participating in the implementation of new protocols; administering standard and nonstandard research interventions; evaluating the patient’s response to intervention and making decisions around patient safety and participation; responding to variances in protocol implementation and reporting variances to the research team;

implementing and adhering to established safety protocols for patient and research participant interactions, utilizing clinical judgment to identify and escalate potential safety issues appropriately; evaluating patient outcomes and providing clinical care and judgement of research activities within scope of practice; collaborating with the research team and delivery system partners within the scope of the intervention; and implementing quality improvement activities in the team.

• Pursues effective relationships with others by proactively providing resources, information, advice, and expertise with coworkers and members. Listens to, seeks, and addresses performance feedback; provides mentoring to team members. Pursues self-development; creates plans and takes action to capitalize on strengths and develop weaknesses; influences others through technical explanations and examples. Adapts to and learns from change, challenges, and feedback; demonstrates flexibility in approaches to work;
  
  helps others adapt to new tasks and processes. Supports and responds to the needs of others to support a business outcome.
• Completes work assignments autonomously by applying up-to-date expertise in subject area to generate creative solutions; ensures all procedures and policies are followed; leverages an understanding of data and resources to support projects or initiatives. Collaborates cross-functionally to solve business problems; escalates issues or risks as appropriate; communicates progress and information. Supports, identifies, and monitors priorities, deadlines, and expectations. Identifies, speaks up, and implements ways to address improvement opportunities for team.
• Works on budgeting and financing by: developing a working understanding of how to provide input on implementing budget components for internally funded standard and nonstandard projects.
• Conducts clinical research by: independently collecting data in clinical trials (e.g., recruiting human subjects, administering surveys and/experiments); leveraging a comprehensive foundational knowledge of source data and the tools leveraged for analyzing, and interpreting clinical data; leveraging a comprehensive foundational knowledge of clinical trials, studies, and interventions at the site-level; independently contributing to the development of standard and nonstandard clinical research protocols and other processes of clinical trials;
  
  preparing and/or supporting the submission of study documentation to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for executing standard and non-standard 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 standard and non-standard 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).
• Ensures research compliance by: independently drafting and/or preparing and submitting clinical trial applications in compliance and consistency with all applicable federal, state, and local regulations, and reviewing and providing input on KP compliance policies and procedures; identifying compliance and/or quality issues and assisting in the development of corrective action plans, escalating as necessary; identifying opportunities to update…