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Remote Nurse Writer Jobs in Colorado (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

DaVita, Inc.

Nurse Practitioner Educator

Denver, CO · On-site +1

Excellent verbal/written communication and interpersonal skills. * Ability to work independently ... Fully remote with the ability to travel as needed to present in-person training (travel is 2-4 ...

DaVita, Inc.

Nurse Practitioner Educator

Denver, CO · On-site +1

Excellent verbal/written communication and interpersonal skills. * Ability to work independently ... Fully remote with the ability to travel as needed to present in-person training (travel is 2-4 ...

BetterHelp

Licensed Psychologist- Remote

Denver, CO · Remote

$650/wk

Excellent written communication. * Must have professional liability insurance. * Reliable Internet ... Also, we are unable to accept substance abuse counselors, school counselors, registered nurses ...

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Remote Nurse Writer information

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$12

$25

$44

How much do remote nurse writer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for remote nurse writer in Colorado is $25.54, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $29.33 per hour, depending on experience, location, and employer.

What is a remote nurse writer?

A Remote Nurse Writer is a licensed nurse who creates written content related to healthcare, nursing, and medicine. They work from home or another remote location, writing articles, blogs, white papers, patient education materials, and continuing education courses. Their expertise ensures accuracy, credibility, and clarity in healthcare communication. This role may involve freelance, contract, or full-time positions with healthcare organizations, media companies, or educational institutions.

What are some typical daily responsibilities for a remote nurse writer?

As a Remote Nurse Writer, your daily tasks often include researching and crafting articles, educational materials, or patient resources related to healthcare topics, and reviewing documents for clinical accuracy. You’ll frequently collaborate with editorial teams, subject matter experts, and sometimes marketing departments to ensure content meets industry standards and organizational objectives. Many roles also require regular peer review or revision based on feedback and maintaining compliance with healthcare regulations. The job offers flexibility, but strong self-motivation and organizational skills are important to meet deadlines and manage multiple projects efficiently.

What are the key skills and qualifications needed to thrive in the remote nurse writer position, and why are they important?

To thrive as a Remote Nurse Writer, you need clinical nursing experience, strong writing skills, and a solid understanding of medical terminology, often supported by a registered nursing license. Familiarity with content management systems, digital research tools, and healthcare compliance guidelines like HIPAA is typically required. Excellent time management, attention to detail, and the ability to communicate complex information clearly set standout candidates apart. These competencies are crucial for producing accurate, trustworthy content that effectively educates both healthcare professionals and patients in a remote, deadline-driven environment.

What are the most commonly searched types of Nurse Writer jobs in Colorado?

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

What are popular job titles related to Remote Nurse Writer jobs in Colorado?

For Remote Nurse Writer jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Remote Nurse Writer jobs in Colorado look for?

The top searched job categories for Remote Nurse Writer jobs in Colorado are:

What cities in Colorado are hiring for Remote Nurse Writer jobs?

Cities in Colorado with the most Remote Nurse Writer job openings:

Remote Nurse Writer jobs near you
Infographic showing various Remote Nurse Writer job openings in Colorado as of August 2026, with employment types broken down into 76% Full Time, 6% Part Time, and 18% Contract. Highlights an 100% Remote job distribution, with an average salary of $53,122 per year, or $25.5 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Denver, CO • On-site, Remote

$143K - $238K/yr

Full-time

Posted 4 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 493 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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