Research Specialist III (28 hours/week Silverdale)

Kaiser Permanente; Silverdale (WA); On-site; USD 60,000 - 85,000; Part time

Job summary

Kaiser Permanente is seeking a Research Specialist III to support a CDC study evaluating flu vaccine effectiveness in patients at Kaiser Permanente Washington urgent care clinics. The role lasts about 4–6 months during flu season and involves reviewing EPIC schedules, screening, consenting, and collecting nose/throat swabs.

The ideal candidate is detail-oriented, able to work independently and with a team, and experienced in recruiting participants in clinical settings; diversity in applicants

Qualifications

• Bachelors degree in Public Health, Health Care Administration, Epidemiology, Health Sciences, or related field.
• Minimum 2 years in health research/public health or 5 years in a related field; or equivalent combination.

Responsibilities

• Assist day-to-day operations of research projects and ensure IRB protocol compliance.
• Screen, consent, enroll participants and collect data and specimens as needed.
• Prepare data reports, monitor study progress and identify data quality issues.
• Draft recruitment and data collection materials and assist in study documentation.
• Coordinate with cross-functional teams to support study goals.

Skills

Ambiguity Mgmt

Attention to Detail

Communication

Critical Thinking

Teamwork

Decision Making

Diversity & Inclusion

Learning Agility

Organizational Savvy

Problem Solving

Stakeholder Mgmt

Health Care Industry

Education

Bachelor's Degree

Master's Degree (Preferred)

Job description

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 Specialist III 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.

Job Summary:

Assists with research support by implementing day-to-day operations of projects, monitoring resources for research studies, and following federal and local regulations, standard operating procedures, and Institutional Review Board (IRB) approved protocols. Contributes to the execution of research by independently conducting data gathering activities, preparing data reports for accuracy and identifying inconsistencies in data, and performing complex tasks related to the recruitment, enrollment, consenting, follow-up with participants, and answering participant questions. Contributes to the development of research materials and procedures by drafting study materials (e.g., recruitment, data collection, retention) in a variety of formats including online. Assists in the documentation and reporting of research study activities by assisting the development of tools, systems, and forms for project tracking and documentation, documenting study progress, and escalating issues to project managers or investigators.

Essential Responsibilities:

• 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.
• Contributes to the execution of research studies by: independently conducting research surveys, focus groups, qualitative interviews, or other data gathering activities for moderately complex projects; training others on project support activities (e.g., data collection, administering informed consent, conducting procedures); preparing open-ended/qualitative data for analysis and building analytical datasets; preparing data reports and identifying data quality issues; performing complex tasks related to the recruitment, enrollment, consenting, and follow-up with participants; and answering participant questions regarding basic and/or complex studies and escalating issues if necessary.
• Contributes to the development of research materials and procedures by: drafting study materials (e.g., recruitment, data collection, retention) in a variety of formats including online.
• Assists in the documentation and reporting of research study activities by: assisting the development of tools, systems, and forms for project tracking and documentation; and documenting the progress of study activities and escalating issues to project managers or investigators.
• Assists with research support operations by: implementing day-to-day operations of projects; monitoring resources for research studies; contributing to and/or assisting the management of project budgets; performing literature reviews and/or contributing to the development of grant proposals; contributing to drafts of Institutional Review Board (IRB) protocols, amendments, continuing reviews, and other documentation; contributing to drafts of Institutional Review Board (IRB) protocols, amendments, continuing reviews, and other documentation; and following federal and local regulations, standard operating procedures, and IRB approved protocols and maintaining compliance for handling research data.

Knowledge, Skills and Abilities: (Core)

• Ambiguity/Uncertainty Management
• Attention to Detail
• Business Knowledge
• Communication
• Critical Thinking
• Cross-Group Collaboration
• Decision Making
• Dependability
• Diversity, Equity, and Inclusion Support
• Drives Results
• Facilitation Skills
• Health Care Industry
• Influencing Others
• Integrity
• Learning Agility
• Organizational Savvy
• Problem Solving
• Short- and Long-term Learning & Recall
• Teamwork
• Topic-Specific Communication

Knowledge, Skills and Abilities: (Functional)

• Confidentiality
• Good Clinical Practices (GCP)
• Health Care Compliance
• Health Care Policy
• Research & Evaluation Data Collection
• Research & Evaluation Study Design
• Research Ethics
• Stakeholder Management

Minimum Qualifications:

• Bachelors degree in Public Health, Health Care Administration, Epidemiology, Health Sciences, Social or Behavioral Sciences, Health Services, Statistics, or Health Economics, or related field AND minimum two (2) years of experience in health research, public health, laboratory or social science research setting, epidemiology, social or behavioral sciences, health services or a directly related field OR Minimum five (5) years of experience in health research, public health, laboratory or social science research setting, epidemiology, social or behavioral sciences, health services or a directly related field.

Preferred Qualifications:

• Master's degree in Public Health, Health Care Administration, Epidemiology, Health Sciences, Social or Behavioral Sciences, Health Services, Statistics, or Health Economics, or related field.