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Philips

User Experience Research Specialist (Bothell, WA)

Posted 4 Days Ago
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In-Office
Bothell, WA
80K-127K Annually
Mid level
In-Office
Bothell, WA
80K-127K Annually
Mid level
Manage end-to-end user and product research for Philips Sonicare, including participant recruitment and database growth, study setup, IRB submissions, and maintenance of study documentation. Ensure compliance with QMS, GCP, and GDP in a regulated medical device environment. Coordinate participant experience, logistics, equipment and supplies, drive process standardization and continuous improvement, and partner with Privacy and global research teams to scale research practices and insights.
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Job TitleUser Experience Research Specialist (Bothell, WA)

Job Description

User Experience Research Specialist (Bothell, WA)

As a User Experience Research Specialist, you will contribute to the development of next-generation products and digital innovations for Philips Sonicare. In this role, you will oversee the operational aspects of user research within Research and Development, ensuring excellence in participant database management, participant experience, safety, quality, and compliance.

Your role:

  • Support end-to-end user product research activities, from study setup through insight delivery, including documentation review, participant coordination, and synthesis of insights using repositories and literature reviews to identify patterns and important trends across studies.
  • Lead participant recruitment and engagement by developing study materials, screening for eligibility, scheduling sessions, and serving as the primary point of contact—ensuring a seamless and positive participant experience while troubleshooting issues in real time.
  • Build and grow a diverse participant database through multi-channel sourcing strategies (e.g., social media, referrals, professional networks, and events) to support ongoing and future research needs.
  • Ensure compliance with Quality Management System (QMS), regulatory standards, and privacy laws by applying Good Clinical Practice (GCP) and Good Documentation Practice (GDP), maintaining audit readiness within a regulated medical device environment.
  • Manage Institutional Review Board (IRB) submissions and study documentation, including consent, eligibility verification, and maintenance of Trial Master Files and Site Regulatory Files in close partnership with researchers and Research Operations.
  • Drive continuous improvement by standardizing processes, optimizing workflows, and developing tools and templates that enable efficient, compliant, and privacy-first research practices.
  • Collaborate with the facilities team to manage inventory, order and restock supplies, maintain and calibrate equipment, ensuring continuous improvement and audit readiness
  • Partner with Privacy stakeholders and Research Operations leadership to design, standardize, and optimize processes, tools, and templates that ensure efficient, compliant, and privacy-first practices develop and improve processes and templates to ensure privacy and compliance in an efficient manner. Coordinate with global research teams to share best practices, align on methodologies, and leverage cross-regional sties and participant capabilities to scale and enhance research impact

You're the right fit if:

  • You’ve acquired 3+ years of experience in User Research or Clinical Research (preferably hands-on experience).
  • Your skills include:
    • Proven track record of compliance with Good Clinical Practice and Good Documentation Practice.
    • Proficient in Microsoft Office; Copilot, Power Automate, and Power BI are nice to have.
    • Experience with EyeQuestion, Veritas IRB, UserTesting.com, Tremendous,  Smartsheet, Medidata, E-TMF, EDC preferred.
    • Experience in administrative duties including but not limited to: participant communication, scheduling, reminders and compensation, accurate accounting and reconciliation of participant compensation, develop and maintain a database of qualified participants both locally and nationally.
    • Strong understanding of (user and/or clinical) research processes.
    • Experience with continuous improvement projects.
    • Experience with medical devices, nice to have.
  • You have a Bachelor’s Degree in Business / Administration, Healthcare, Sciences, Design, Human Factors, Psychology, Behavioral Sciences, Sensory Science, Ergonomics, Human Computer Interaction, Engineering and/or Dentistry or a related field, OR equivalent combination of education and above listed experience.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
  • You have a strong drive to put the consumer and study participants first, and have the ability to communicate with study participants in a professional manner that represents the Philips brand. You have strong decision-making skills, and can identify and resolve problems in a timely manner. You have excellent organizational skills, with extreme attention to detail. You thrive in a fast-paced and ever-changing environment. You are a self-starter, who collaborates well with a team, and excel both in teaching and enforcing rules and regulations as needed.

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is an office role.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Learn more about our culture.

Philips Transparency Details

The pay range for this position in Washington is $80,000 to $127,000.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.   

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered.  Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found here. 

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. 

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position.  For this position, you must reside in or within commuting distance to Bothell, WA.

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates.  Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.

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