Research Nurse Interventionist- TACOMA
Utilizes professional clinical skills, education and/or experience in project planning and implementation of data collection for complex clinical/health research trials. Utilizes professional clinical skills/training for independent decision making for data collection/trial intervention(s)/evaluation. The scope of responsibility for a Research Interventionist is greater than that for a Clinical Research Specialist due to any combination of the following: greater level of independent safety or clinical decision making required; greater level of specialized clinical knowledge required; substantial contribution to areas such as project intervention materials, plans, study design and research papers; and comprehensive consultation role on policies and methodology.
Essential Responsibilities:
- Performs clinical evaluation/intervention/measurements requiring professional clinical knowledge/education/training. Utilizes clinical knowledge and skills to evaluate participant responses and make subsequent decisions around patient safety and participation issues.
- Provides professional expertise in day-to-day coordination of research activities. Develops project intervention plans and tools, data collection instruments, manual of operations, trains new employees, prepares reports, etc. Plans, implements and monitors participant safety and data quality control measures.
- Evaluates responses of participants and makes independent clinical judgments regarding responses to clinical intervention.
- Participates as part of the research project team, attends project meetings, and identifies problems and proposes solutions.
- May perform medical record review requiring professional clinical background/education/ experience for correct interpretation and data collection.
- May perform telephone interviews, in-person interviews or physical assessments requiring professional clinical background/education.
- Minimum two (2) years of experience performing professional functions required by the project.
- High School Diploma or General Education Development (GED) required.
- N/A
- Experience with individual and/or group counseling and/or facilitation, and related research experience.
- Knowledge of research data collection requirements and specialized clinical intervention/measurement/assessment skills as required by the projects.
- A thorough understanding of regulatory policies governing industry practices, HIPAA requirements for clinical research, and knowledgeable about patient safety and quality control requirements.
- Excellent written and verbal communication skills, organizational skills and interpersonal skills.
- Continual updating of skills and knowledge related to research.
- Masters degree or PhD in health-related field.
- Certifications, licenses, or degrees as determined by the needs of the research projects, such as, registered nurse, nurse practitioner, certified mental health therapist/specialist, MSW, pharmacist, physical therapist, certified health education specialist, clinical psychologist, acupuncturist as applicable to research project and field of study by date of hire/transfer.
Kaiser Permanente is an equal opportunity employer committed to fair, respectful, and inclusive workplaces. Applicants will be considered for employment without regard to race, religion, sex, age, national origin, disability, veteran status, or any other protected characteristic or status.
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