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Senior Science Writer Jobs in Seattle, WA (NOW HIRING)

As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners ...

The Senior Scientist in the Cell Science Department is responsible for the development and ... Write and review Standard Operating Procedures (SOPs) and technical reports for regulatory filings.

Partner with departmental leadership, faculty investigators, Research Operations, Data Science, and ... Excellent written, verbal, and interpersonal communication skills. Preferred Qualifications

Senior Applied Scientist

Seattle, WA · On-site

$150 - $210/hr

As a Senior Applied Scientist on the team, you will independently own complex evaluation work from ... This is hands-on applied science. You will write high-quality code, work with large and imperfect ...

The Senior Director will serve as a senior scientific partner to Clinical Development, Regulatory ... Strong scientific writing, communication, and presentation skills. * Demonstrated ability to work ...

New

Work will be conducted on-site at the Northwest Fisheries Science Center, Seattle, Washington (WA ... Write technical reports and status updates, contribute to peer-reviewed manuscripts, and present ...

Senior Applied Scientist - Moloco Ads

Seattle, WA · On-site

$104K - $142K/yr

Learn from your senior peers how to identify new areas to improve our infrastructure and machine ... At least 4 years of engineering or applied science experience * Proficient verbal and written ...

Senior Applied Scientist

Seattle, WA · On-site

$104K - $142K/yr

As a Senior Applied Scientist on the team, you will independently own complex evaluation work from ... This is hands-on applied science. You will write high-quality code, work with large and imperfect ...

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Showing results 1-20

Senior Science Writer information

See Seattle, WA salary details

$34.7K

$105.3K

$194.6K

How much do senior science writer jobs pay per year?

As of Sep 3, 2026, the average yearly pay for senior science writer in Seattle, WA is $105,335.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,800.00 and $114,900.00 per year, depending on experience, location, and employer.

What is a senior science writer?

A Senior Science Writer is a professional who creates and edits scientific content for various audiences, including researchers, policymakers, and the general public. They work closely with scientists, subject matter experts, and communication teams to translate complex scientific information into clear, engaging, and accurate materials. Their work may include writing articles, reports, press releases, white papers, and grant proposals. They often have a background in science or journalism and must possess strong writing, research, and editing skills. Depending on the organization, they may also oversee junior writers, manage projects, and ensure consistency in scientific messaging.

What are typical daily responsibilities for a senior science writer?

A Senior Science Writer typically drafts and edits articles, research summaries, press releases, and technical documents for print or digital publication. They often interview scientists, attend research meetings, and translate complex data into accessible language for various audiences. Collaboration with editors, graphic designers, and subject matter experts is common to ensure accuracy and engaging presentation. Additionally, Senior Science Writers may mentor junior writers, contribute to editorial strategy, and help coordinate publication schedules, offering a dynamic and multifaceted work environment.

What are the key skills and qualifications needed to thrive as a senior science writer?

To thrive as a Senior Science Writer, you need exceptional writing and editing skills, advanced scientific literacy (often supported by a degree in a science discipline), and a proven track record in science communication. Familiarity with publishing platforms, reference management tools, and proficiency in editing or style guide systems (such as AMA or APA) is commonly expected. Outstanding soft skills include attention to detail, the ability to translate complex concepts for diverse audiences, project management, and collaborative teamwork. These capabilities ensure scientifically accurate, engaging content that meets both editorial standards and audience needs, while supporting collaboration with subject matter experts.

What are the most commonly searched types of Science Writer jobs in Seattle, WA?

The most popular types of Science Writer jobs in Seattle, WA are:

What are popular job titles related to Senior Science Writer jobs in Seattle, WA?

For Senior Science Writer jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Senior Science Writer jobs in Seattle, WA look for?

The top searched job categories for Senior Science Writer jobs in Seattle, WA are:

Infographic showing various Senior Science Writer job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 22% Part Time, and 4% Contract. Highlights an 76% Physical, 5% Hybrid, and 19% Remote job distribution, with an average salary of $105,335 per year, or $50.6 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Seattle, WA • On-site, Remote

$143K - $238K/yr

Full-time

Posted 17 days ago


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

133rd of 496 rated machine equipment manufacturers


Job description

Work Flexibility: Remote

Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.

As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.

What You Will Do

  • Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.

  • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.

  • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

  • Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.

  • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.

  • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.

  • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.

What You Need

Required

  • Bachelor's degree in a scientific, technical, healthcare, or related discipline.

  • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.

  • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.

  • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.

  • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.

  • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.

  • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.

Preferred

  • Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

  • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.

  • Experience supporting regulatory submissions and global market access initiatives for medical devices.

  • Knowledge of clinical operations, risk management, and international regulatory requirements.

United States of America Pay Ranges:

  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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