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Philips

Makes medical devices and personal health products

Senior Clinical Development Scientist / Medical Safety Manager

Clinical Research Operations +1Confirmed live in the last 24 hours
Full-timeBothell, WA, USA$149k - $237k

About the Job

Requirements

  • Have 7 or more years of experience in the medical device industry or a similar industry performing medical safety risk assessments and/or conducting clinical research on medical devices.
  • Have strong knowledge of relevant standards and regulations for the medical device industry, including ISO and IEC.
  • Have strong knowledge and understanding of Health Hazard Evaluations, Issue Impact Assessments, and Risk-Benefit Analyses, including how to conduct them in a medical device environment.
  • Have a strong understanding of clinical research as it relates to the medical device industry and its relevant standards.
  • Have a doctoral degree in Dentistry or a Dental Hygienist background, or a PhD in scientific research in the medical devices space.
  • Be able to successfully perform the minimum Physical, Cognitive and Environmental job requirements with or without accommodation.
  • Communicate effectively and influence cross-functional stakeholders using clinical expertise and knowledge of standard of care and medical device standards.
  • Have US work authorization; candidates who require sponsorship for a work-authorized visa now or in the future will not be considered.
  • Reside in or within commuting distance to Bothell, Washington.

Responsibilities

  • Support clinical evidence generation, clinical development strategy, and medical safety activities across the product lifecycle, contributing to patient safety, regulatory compliance, and evidence-based decision-making.
  • Analyze clinical trial protocols and clinical studies to support clinical development, ensuring clinical data integrity, scientific rigor, and reliable interpretation of study results.
  • Evaluate safety information from clinical studies, post-market surveillance, literature reviews, real-world data, and other safety surveillance sources; identify potential safety risks and support ongoing safety monitoring.
  • Collaborate with multidisciplinary teams on New Product Introduction projects, post-market initiatives, risk-benefit analyses, safety surveillance, and regulatory documentation; provide clinical and medical safety input throughout the product lifecycle.
  • Support evidence dissemination and scientific communications with internal stakeholders, external investigators, Key Opinion Leaders, and cross-functional partners; translate clinical and safety findings into clear information that supports alignment and informed decisions.

Desired Qualifications

  • Experience in the oral healthcare or dentistry space is highly preferred.
  • A doctoral degree in Dentistry or a Dental Hygienist background is strongly preferred.

About the Company

Philips

Makes medical devices and personal health products

Philips makes medical equipment and software for hospitals and care providers, along with personal health products for consumers. Its hospital portfolio spans MRI and CT scanners, ultrasound, image-guided treatment systems and patient monitors, while Sonicare and Avent cover oral health and baby care. Clinical software connects medical images and patient data across care teams, and the company earns revenue from equipment, software, maintenance and consumer product sales. It works with health systems through long-term technology and service partnerships, including solutions for care at home. Founded in 1891, Philips is headquartered in Amsterdam, the Netherlands.

Company size
10,001+
Company stage
Acquired
Total funding
$164.7M
Headquarters
Andover, MN
Founded
1891

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