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Senior Science Writer Jobs in Colorado (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 ...

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 ...

Senior Machine Learning Scientist

Boulder, CO · On-site +1

$96K - $131K/yr

What sets Flagship apart is our ability to advance science and technology by uniting innovation ... Strong technical writing and communication skills, including reports, presentations, and peer ...

Senior Machine Learning Scientist

Boulder, CO · On-site +1

$96K - $131K/yr

What sets Flagship apart is our ability to advance science and technology by uniting innovation ... Strong technical writing and communication skills, including reports, presentations, and peer ...

Degree should be in biological science, English or other relevant area. 5 to 7 years directly related medical writing experience. Outstanding writing, analytical and research skills a must. Ability ...

Our mission is to deliver high-quality service and technology solutions - rooted in strong science ... Write and edit clinical development documents, including but not limited to, clinical protocols ...

Strong written & oral communication skills * Strong organizational and collaboration skills ... With active engagements spanning pharmaceuticals, material science, financial services, government ...

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Senior Science Writer information

See Colorado salary details

$32.1K

$97.3K

$179.8K

How much do senior science writer jobs pay per year?

As of Aug 29, 2026, the average yearly pay for senior science writer in Colorado is $97,328.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,700.00 and $106,200.00 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 Colorado?

The most popular types of Science Writer jobs in Colorado are:

What cities in Colorado are hiring for Senior Science Writer jobs?

Cities in Colorado with the most Senior Science Writer job openings:

Infographic showing various Senior Science Writer job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, 1% Temporary, and 2% Contract. Highlights an 73% Physical, 4% Hybrid, and 23% Remote job distribution, with an average salary of $97,328 per year, or $46.8 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Denver, CO • On-site, Remote

$143K - $238K/yr

Full-time

Posted 11 days ago


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

130th of 495 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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