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Principal Medical Writer

Thermo Fisher Scientific

Healthcare Jobs

Principal Medical Writer

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Principal Medical Writing - Make an Impact at the Forefront of Innovation
As a Principal Medical Writer, you will serve as the primary author by writing and providing input on routine documents such as clinical study reports and study protocols and summarizes data from clinical studies.


What You'll Do:
• Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.
• As the lead writer, review documents for the team and provide training and guidance to junior team members.
• Provide advice on document development strategy, regulations and industry best practices.
• Demonstrate subject matter and therapeutic area expertise.
• Act as backup program manager.
• Collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

Education & Experience Requirements:
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
• Experience within regulatory medical writing (comparable to 8+ years) required
• Experience working in the pharmaceutical/CRO industry preferred
• Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.


Knowledge, Skills, Abilities:
• Significant knowledge of global, regional, national and other document development guidelines
• In-depth knowledge in one or more specialty areas such as preclinical, therapeutic, regulatory, submissions, communications, etc.
• Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
• Excellent project management skills
• Advanced interpersonal, oral and written communication, and presentation skills
• Excellent negotiation skills
• Excellent judgment; high degree of independence in decision making and problem solving
• Ability to mentor and lead junior level staff.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Locations

  • Beijing, Beijing, China

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 CNY / yearly

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

Skills Required

  • medical writingintermediate
  • data interpretationintermediate
  • project managementintermediate
  • interpersonal communicationintermediate
  • negotiationintermediate
  • mentoringintermediate
  • knowledge of global document development guidelinesintermediate
  • grammatical and proofreading skillsintermediate

Required Qualifications

  • Bachelor's degree in scientific discipline (advanced degree preferred) (experience)
  • 8+ years regulatory medical writing experience (experience)
  • pharmaceutical/CRO industry experience preferred (experience)
  • AMWA/EMWA/RAC qualifications advantageous (experience)

Responsibilities

  • Provide high-quality medical and scientific writing
  • Review documents and train junior team members
  • Provide advice on document development strategy and regulations
  • Demonstrate subject matter and therapeutic area expertise
  • Act as backup program manager
  • Collaborate with internal and external clients

Benefits

  • general: part of global team
  • general: values passion innovation and scientific excellence
  • general: collaboration and development environment

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Thermo Fisher Scientific logo

Principal Medical Writer

Thermo Fisher Scientific

Healthcare Jobs

Principal Medical Writer

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Principal Medical Writing - Make an Impact at the Forefront of Innovation
As a Principal Medical Writer, you will serve as the primary author by writing and providing input on routine documents such as clinical study reports and study protocols and summarizes data from clinical studies.


What You'll Do:
• Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.
• As the lead writer, review documents for the team and provide training and guidance to junior team members.
• Provide advice on document development strategy, regulations and industry best practices.
• Demonstrate subject matter and therapeutic area expertise.
• Act as backup program manager.
• Collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

Education & Experience Requirements:
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
• Experience within regulatory medical writing (comparable to 8+ years) required
• Experience working in the pharmaceutical/CRO industry preferred
• Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.


Knowledge, Skills, Abilities:
• Significant knowledge of global, regional, national and other document development guidelines
• In-depth knowledge in one or more specialty areas such as preclinical, therapeutic, regulatory, submissions, communications, etc.
• Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
• Excellent project management skills
• Advanced interpersonal, oral and written communication, and presentation skills
• Excellent negotiation skills
• Excellent judgment; high degree of independence in decision making and problem solving
• Ability to mentor and lead junior level staff.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Locations

  • Beijing, Beijing, China

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 CNY / yearly

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

Skills Required

  • medical writingintermediate
  • data interpretationintermediate
  • project managementintermediate
  • interpersonal communicationintermediate
  • negotiationintermediate
  • mentoringintermediate
  • knowledge of global document development guidelinesintermediate
  • grammatical and proofreading skillsintermediate

Required Qualifications

  • Bachelor's degree in scientific discipline (advanced degree preferred) (experience)
  • 8+ years regulatory medical writing experience (experience)
  • pharmaceutical/CRO industry experience preferred (experience)
  • AMWA/EMWA/RAC qualifications advantageous (experience)

Responsibilities

  • Provide high-quality medical and scientific writing
  • Review documents and train junior team members
  • Provide advice on document development strategy and regulations
  • Demonstrate subject matter and therapeutic area expertise
  • Act as backup program manager
  • Collaborate with internal and external clients

Benefits

  • general: part of global team
  • general: values passion innovation and scientific excellence
  • general: collaboration and development environment

Target Your Resume for "Principal Medical Writer" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Principal Medical Writer. Takes only 15 seconds!

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

Check Your ATS Score for "Principal Medical Writer" , Thermo Fisher Scientific

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

Answer 10 quick questions to check your fit for Principal Medical Writer @ Thermo Fisher Scientific.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.