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Remote Contract Medical Writer Jobs in Oregon (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 remotely anywhere within the United States. Stryker is one of the world's leading medical technology ...

New

micro1 AI

Medical Writing Manager

Salem, OR · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Bend, OR · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Beaverton, OR · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Portland, OR · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Gresham, OR · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Eugene, OR · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Hillsboro, OR · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

Verve

Data Engineer (Remote / Contract)

OR · On-site +1

$114K - $137K/yr

This is a fully remote, 40-hour per week contract position with the opportunity to shape the future ... You are comfortable writing SQL and manipulating large structured or unstructured datasets for ...

New

Spyre Therapeutics

Associate Director, Medical Writing

OR · On-site +1

$170K - $199K/yr

As Associate Director, Medical Writer, you will lead or make key contributions to clinical and ... Remote working environment with frequent in-person meetings to address complex problems and build ...

Travere

Associate Director, Medical Writing

OR · On-site +1

San Diego, United Kingdom - Remote, USA- Remote Be a part of a global team that is inspired to make ... Contract Research Organization (CRO) or related environment. Additional Skills/Experience ...

micro1 AI

Medical Billing Specialist

Bend, OR · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on developing advanced AI-assisted writing tools for clinical documentation. In ...

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Remote Contract Medical Writer information

What is a remote contract medical writer?

A Remote Contract Medical Writer is a professional who creates scientific documents, such as clinical study reports, regulatory submissions, or educational materials, for pharmaceutical, biotech, or healthcare organizations while working remotely on a contract basis. They translate complex medical data into clear, accurate, and compliant content tailored to the target audience, such as regulatory agencies, healthcare providers, or patients. These writers typically collaborate with subject matter experts, researchers, and regulatory teams, and their work often follows strict industry guidelines and deadlines. Remote contract roles offer flexibility and the ability to work with multiple clients from different locations.

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

To thrive as a Remote Contract Medical Writer, you need a strong background in life sciences, excellent research abilities, and proven writing skills, often supported by a relevant degree or advanced certification. Familiarity with regulatory documentation, referencing software (such as EndNote), and platforms like Microsoft Office or document management systems is typically required. Keen attention to detail, time management, and clear communication are essential soft skills for meeting deadlines and collaborating remotely. These skills ensure the creation of accurate, compliant, and high-quality medical documents for clients and regulatory agencies.

What are some common challenges faced by remote contract medical writers, and how can they be managed?

Remote contract medical writers often encounter challenges such as managing multiple deadlines for different clients, adapting to varying writing styles and guidelines, and maintaining clear communication across virtual teams. To address these, it’s important to develop strong organizational skills, set clear expectations with clients, and utilize project management tools. Regular check-ins and proactive communication with clients and collaborators help ensure alignment and smooth workflow.

What is the difference between Remote Contract Medical Writer vs Remote Full-Time Medical Writer?

AspectRemote Contract Medical WriterRemote Full-Time Medical Writer
CredentialsTypically requires medical or scientific degrees, writing experience, and industry certificationsSame as contract; often requires similar credentials and certifications
Work EnvironmentProject-based, flexible hours, short-term engagementsPermanent employment, consistent schedule, ongoing projects
Employer & Industry UsageFreelance or consulting firms, biotech, pharma companiesPharmaceutical companies, CROs, biotech firms
Search & Comparison IntentHigh overlap in skills, project scope, and industry contextSimilar roles with different employment types

The main difference between a Remote Contract Medical Writer and a Remote Full-Time Medical Writer lies in employment type and engagement duration. Contract writers work on specific projects with flexible hours, while full-time writers have ongoing employment with consistent schedules. Both roles require similar credentials and industry experience, making them comparable in skills and responsibilities.

What are the most commonly searched types of Remote Medical Writer jobs in Oregon?

The most popular types of Remote Medical Writer jobs in Oregon are:

What are popular job titles related to Remote Contract Medical Writer jobs in Oregon?

For Remote Contract Medical Writer jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Remote Contract Medical Writer jobs in Oregon look for?

The top searched job categories for Remote Contract Medical Writer jobs in Oregon are:

What cities in Oregon are hiring for Remote Contract Medical Writer jobs?

Cities in Oregon with the most Remote Contract Medical Writer job openings:

Remote Contract Medical Writer jobs near you

Senior Staff Medical Writer (Remote)

Stryker

Portland, OR • On-site, Remote

$143K - $238K/yr

Full-time

Posted 3 days ago

New

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

131st of 491 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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