Research Specialist III, Research Support

Kaiser Permanente

Pleasanton, Northern (CA, KY)

Hybrid

USD 55,000 - 85,000

Full time

2 days ago
Be an early applicant
Application generator

Get a reply from this employer — a resume and cover letter tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Kaiser Permanente in Pleasanton, CA is seeking a Research Support Specialist to help implement day-to-day operations of projects and monitor regulatory compliance. You will conduct data gathering, prepare reports, recruit and enroll participants, and draft study materials under IRB protocols.

You will also assist in documenting study activities, developing tools for tracking progress, and escalating issues to project managers. Strong attention to detail and collaboration are essential.

Qualifications

  • Bachelor's 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.

Responsibilities

  • Supports and maintains effective relationships with coworkers and stakeholders to enable project success.
  • Performs autonomous data gathering, data preparation, and reporting.
  • Contributes to recruitment, enrollment, consent, follow-up, and participant questions.
  • Assists in drafting study materials and online recruitment tools.
  • Maintains documentation and reporting of study activities and escalates issues as needed.
  • Ensures compliance with federal/local regulations and IRB protocols.

Skills

Attention to Detail
Communication
Cross-Group Collaboration
Problem Solving
Leadership
Learning Agility
Adaptability
Teamwork
Decision Making
Critical Thinking
Diversity & Inclusion
Integrity
Health Care Industry
Research Knowledge

Education

Bachelor's degree in Public Health or related field
Master's degree (preferred)

Job description

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.
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Research Specialist II, Research Support
Research Specialist II, Research Support

Kaiser Permanente • Chino Hills (CA)

On-site
USD 65,000 - 90,000
Research Specialist V, Research Support
Research Specialist V, Research Support

Kaiser Permanente • Pleasanton (CA), Northern (KY)

Hybrid
USD 95,000 - 145,000
Research Specialist III (28 hours/week Silverdale)
Research Specialist III (28 hours/week Silverdale)

Kaiser Permanente • Silverdale (WA)

On-site
USD 60,000 - 85,000
Research Specialist II, Clinical Laboratory Support (Durational with Benefits)
Research Specialist II, Clinical Laboratory Support (Durational with Benefits)

Kaiser Permanente • Pasadena (CA)

On-site
USD 70,000 - 90,000
Clinical Research Coordinator III, Clinical Trials (Durational with Benefits)
Clinical Research Coordinator III, Clinical Trials (Durational with Benefits)

Kaiser Permanente • San Diego (CA)

On-site
USD 70,000 - 90,000
Research Specialist
Research Specialist

HealthPartners • Saint Louis Park (MN)

On-site
USD 52,000 - 75,000
Research Specialist
Research Specialist

HealthPartners, Inc. • Minnesota

On-site
USD 65,000 - 90,000
Clinical Research Coordinator II, Clinical Trials- San Rafael
Clinical Research Coordinator II, Clinical Trials- San Rafael

Kaiser Permanente • San Rafael (CA)

On-site
USD 60,000 - 90,000
Research Nurse IV, LPN/LVN, Clinical Trials
Research Nurse IV, LPN/LVN, Clinical Trials

Kaiser Permanente • Lancaster (CA)

On-site
USD 90,000 - 130,000
Research Nurse IV, LPN/LVN, Clinical Trials
Research Nurse IV, LPN/LVN, Clinical Trials

Kaiser Permanente • Los Angeles (CA)

Hybrid
USD 90,000 - 120,000