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Remote Regulatory Writing Jobs in Portland, OR (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... writing, medical writing, clinical research, or related regulatory documentation activities.

micro1 AI

Accountant - Remote

Beaverton, OR · Remote

$20 - $30/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

Accountant - Remote

Gresham, OR · Remote

$20 - $30/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

Accountant - Remote

Vancouver, WA · Remote

$20 - $30/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

Accountant - Remote

Portland, OR · Remote

$20 - $30/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

Accountant - Remote

Hillsboro, OR · Remote

$20 - $30/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

CPA - Tax Consultant - Remote

Gresham, OR · Remote

$65 - $70/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

CPA - Tax Consultant - Remote

Portland, OR · Remote

$65 - $70/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

CPA - Tax Consultant - Remote

Vancouver, WA · Remote

$65 - $70/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

CPA - Tax Consultant - Remote

Beaverton, OR · Remote

$65 - $70/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

micro1 AI

CPA - Tax Consultant - Remote

Hillsboro, OR · Remote

$65 - $70/hr

Read and interpret sales and use tax statutes and regulations across US state jurisdictions, and ... Write clear, self-contained test scenarios (including edge cases) for failed criteria, with ...

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Showing results 1-20

All JobsRegulatory Writing JobsRemote Regulatory Writing JobsRemote Regulatory Writing Jobs in Portland, OR

Remote Regulatory Writing information

See Portland, OR salary details

$20

$41

$66

How much do remote regulatory writing jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for remote regulatory writing in Portland, OR is $41.96, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $49.71 per hour, depending on experience, location, and employer.

What is remote regulatory writing?

Remote regulatory writing involves preparing and reviewing documents required for regulatory submissions to agencies like the FDA or EMA, such as clinical study reports, protocols, and investigator brochures. Regulatory writers ensure that all documents comply with industry standards and legal requirements, and they often work for pharmaceutical, biotech, or medical device companies. The 'remote' aspect means that professionals perform these tasks from home or another off-site location, using digital tools to collaborate with teams. This role requires strong scientific knowledge, attention to detail, and excellent written communication skills.

How do remote regulatory writers effectively collaborate with cross-functional teams while working from different locations?

Remote regulatory writers often collaborate with clinical, medical, and regulatory affairs teams spread across various regions. Effective communication is facilitated through regular video conferences, shared document platforms, and project management tools. While time zone differences can be a challenge, clear timelines and well-documented feedback processes help ensure everyone stays aligned. Building strong virtual relationships and being proactive in updates are key to maintaining seamless collaboration and delivering high-quality regulatory documents.

What are the key skills and qualifications needed to thrive as a remote regulatory writer, and why are they important?

To thrive as a Remote Regulatory Writer, you need strong scientific or medical writing expertise, attention to detail, and a background in life sciences or a related field, often supported by advanced degrees. Familiarity with regulatory submission platforms, document management systems, and guidelines such as ICH, FDA, and EMA requirements is essential. Excellent communication, time management, and the ability to work independently are crucial soft skills that set top performers apart. These competencies ensure accurate, compliant, and timely regulatory documentation crucial for product approvals and patient safety.

What is the difference between Remote Regulatory Writing vs Remote Medical Writing?

AspectRemote Regulatory WritingRemote Medical Writing
Required CredentialsLife sciences degree, regulatory affairs certifications (e.g., RAPS), scientific backgroundLife sciences or healthcare degree, medical or scientific background, writing experience
Work EnvironmentPharmaceutical/biotech companies, CROs, regulatory consulting firmsPharmaceutical, biotech, medical communications agencies, healthcare organizations
Industry UsageRegulatory submissions, INDs, NDAs, safety reportsClinical study reports, medical education materials, journal articles
Search & Comparison IntentOften compared for regulatory document creation rolesCompared for medical communication and scientific writing roles

Remote Regulatory Writing focuses on preparing documents for regulatory submissions and compliance, requiring regulatory knowledge and certifications. Remote Medical Writing involves creating scientific and medical content for various audiences, emphasizing medical knowledge and writing skills. While both roles involve scientific writing, their primary focus and industry applications differ.

What are popular job titles related to Remote Regulatory Writing jobs in Portland, OR?

For Remote Regulatory Writing jobs in Portland, OR, the most frequently searched job titles are:

What job categories do people searching Remote Regulatory Writing jobs in Portland, OR look for?

The top searched job categories for Remote Regulatory Writing jobs in Portland, OR are:

Remote Regulatory Writing jobs near you

Senior Staff Medical Writer (Remote)

Portland, OR • On-site, Remote

Stryker
Medical Equipment and Supplies Manufacturing • 10K+ employees

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

Great coworkers

People enjoy working here

Good employer

Learn more about Strykerexternal

$143K - $238K/yr

Full-time

Posted 9 days ago

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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