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Clinical Development Scientist

Philips

Clinical Development Scientist

full-timePosted: Jan 13, 2026

Job Description

Job Title

Clinical Development Scientist

Job Description

Clinical Development Scientist, Oral Healthcare


The Clinical Development Scientist will manage the direction and evidence collection of Philips Oral Healthcare products, working with a highly skilled clinical affairs team responsible for driving safe, effective, and delightful oral health care solutions to patients and consumers.

Your role:

  • Designs, analyzes, and optimizes clinical trial protocols and studies, ensuring alignment with regulatory requirements and organizational objectives.
  • Prepares comprehensive Clinical Evaluation Reports, Clinical Study Reports, and regulatory submission documents using advanced software skills while maintaining compliance with internal and external standards.
  • Conducts thorough literature searches, data collection, and analysis to support evidence generation for new and existing products, ensuring data integrity and contributing to scientific publications and market access strategies.
  • Collaborates closely with colleagues, Key Opinion Leaders, and investigators to facilitate the execution of clinical studies, generate robust data, and promote innovation within the clinical development team.
  • Presents and communicates key findings from studies and literature reviews to internal and external stakeholders, supporting informed decision-making and advancing scientific knowledge.

You're the right fit if:

  • You’ve acquired 3+ years of related experience in clinical research (preferred) in MedTech, Medical Device or equivalent. Experience writing Clinical Evaluation Reports (CER) preferred.
  • Your skills include scientific research competencies, ability to learn and own new domains quickly, strong critical thinking skills, familiarity with experimental design (animal, human, or in vitro/device testing), as well as relevant guidelines, regulations, and standards (GCP, ICG, ISO 14155, etc.)
  • You have a PhD or equivalent preferred, master’s degree with equivalent combination of education and experience required.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
  • You’re an analytical thinker with strong communication skills, ability to analyze and interpret data, and possess a strong ability to collaborate with others. You have a strong ability to convey complex scientific information to audiences with varied technical expertise.

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-based 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.

Philips Transparency Details

The pay range for this position in Bothell, WA, is $113,400 to $181,440.

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.

 #LI-PH1

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.

Locations

  • Bothell, Washington, United States of America

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • clinical trial design and analysisintermediate
  • scientific researchintermediate
  • critical thinkingintermediate
  • experimental designintermediate
  • literature searchesintermediate
  • data analysisintermediate
  • regulatory compliance (GCP, ISO 14155)intermediate
  • advanced software skillsintermediate

Required Qualifications

  • 3+ years clinical research experience in MedTech/Medical Device (experience)
  • experience writing Clinical Evaluation Reports (CER) preferred (experience)
  • PhD or equivalent preferred (Master’s with experience) (experience)
  • familiarity with guidelines/regulations (experience)

Responsibilities

  • design, analyze, optimize clinical trial protocols
  • prepare Clinical Evaluation Reports, Study Reports, regulatory submissions
  • conduct literature searches and data collection/analysis
  • collaborate with colleagues, KOLs, investigators
  • present findings to stakeholders
  • support evidence generation for products

Target Your Resume for "Clinical Development Scientist" , Philips

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Tags & Categories

clinical trial design and analysisscientific researchcritical thinkingexperimental designliterature searchesdata analysisregulatory compliance (GCP, ISO 14155)advanced software skillsHealthcare Technology
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Philips logo

Clinical Development Scientist

Philips

Clinical Development Scientist

full-timePosted: Jan 13, 2026

Job Description

Job Title

Clinical Development Scientist

Job Description

Clinical Development Scientist, Oral Healthcare


The Clinical Development Scientist will manage the direction and evidence collection of Philips Oral Healthcare products, working with a highly skilled clinical affairs team responsible for driving safe, effective, and delightful oral health care solutions to patients and consumers.

Your role:

  • Designs, analyzes, and optimizes clinical trial protocols and studies, ensuring alignment with regulatory requirements and organizational objectives.
  • Prepares comprehensive Clinical Evaluation Reports, Clinical Study Reports, and regulatory submission documents using advanced software skills while maintaining compliance with internal and external standards.
  • Conducts thorough literature searches, data collection, and analysis to support evidence generation for new and existing products, ensuring data integrity and contributing to scientific publications and market access strategies.
  • Collaborates closely with colleagues, Key Opinion Leaders, and investigators to facilitate the execution of clinical studies, generate robust data, and promote innovation within the clinical development team.
  • Presents and communicates key findings from studies and literature reviews to internal and external stakeholders, supporting informed decision-making and advancing scientific knowledge.

You're the right fit if:

  • You’ve acquired 3+ years of related experience in clinical research (preferred) in MedTech, Medical Device or equivalent. Experience writing Clinical Evaluation Reports (CER) preferred.
  • Your skills include scientific research competencies, ability to learn and own new domains quickly, strong critical thinking skills, familiarity with experimental design (animal, human, or in vitro/device testing), as well as relevant guidelines, regulations, and standards (GCP, ICG, ISO 14155, etc.)
  • You have a PhD or equivalent preferred, master’s degree with equivalent combination of education and experience required.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
  • You’re an analytical thinker with strong communication skills, ability to analyze and interpret data, and possess a strong ability to collaborate with others. You have a strong ability to convey complex scientific information to audiences with varied technical expertise.

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-based 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.

Philips Transparency Details

The pay range for this position in Bothell, WA, is $113,400 to $181,440.

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.

 #LI-PH1

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.

Locations

  • Bothell, Washington, United States of America

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • clinical trial design and analysisintermediate
  • scientific researchintermediate
  • critical thinkingintermediate
  • experimental designintermediate
  • literature searchesintermediate
  • data analysisintermediate
  • regulatory compliance (GCP, ISO 14155)intermediate
  • advanced software skillsintermediate

Required Qualifications

  • 3+ years clinical research experience in MedTech/Medical Device (experience)
  • experience writing Clinical Evaluation Reports (CER) preferred (experience)
  • PhD or equivalent preferred (Master’s with experience) (experience)
  • familiarity with guidelines/regulations (experience)

Responsibilities

  • design, analyze, optimize clinical trial protocols
  • prepare Clinical Evaluation Reports, Study Reports, regulatory submissions
  • conduct literature searches and data collection/analysis
  • collaborate with colleagues, KOLs, investigators
  • present findings to stakeholders
  • support evidence generation for products

Target Your Resume for "Clinical Development Scientist" , Philips

Get personalized recommendations to optimize your resume specifically for Clinical Development Scientist. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Clinical Development Scientist" , Philips

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

clinical trial design and analysisscientific researchcritical thinkingexperimental designliterature searchesdata analysisregulatory compliance (GCP, ISO 14155)advanced software skillsHealthcare Technology
Quiz Challenge

Answer 10 quick questions to check your fit for Clinical Development Scientist @ Philips.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.