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Internship Remote Medical Writing Jobs in Oregon

This position within the Clinical Center of Excellence (CCOE) reports to the Senior Director, Clinical Compliance and Medical Writing, and will be fully remote. In this role, you will have the ...

Associate Director, Medical Writing

OR · Remote

$164K - $225.50K/yr

Manage medical writers (in-house FTEs, contractors, and external vendors) who are individually ... Strong preference for individuals located on the East Coast** #LI-Remote For applicants in the ...

This is a fully remote role! The Principal Medical Writer will research, create, and edit all documents associated with clinical research. The Principal Medical Writer may operate as the project lead ...

Senior Medical Writer (Remote) Arthrex, Inc. is a global medical device company and a leader in new ... This role will specialize in writing, editing, and reviewing clinical regulatory documents as well ...

Supervise the work of contract and freelance writers and mentor junior medical writers as assigned ... Flexible work models, including remote work arrangements, where possible Apply now for a career ...

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Internship Remote Medical Writing information

See Oregon salary details

$9

$16

$23

How much do internship remote medical writing jobs pay per hour?

As of May 28, 2026, the average hourly pay for internship remote medical writing in Oregon is $16.44, according to ZipRecruiter salary data. Most workers in this role earn between $13.22 and $18.56 per hour, depending on experience, location, and employer.

What is an Internship Remote Medical Writing job?

An Internship Remote Medical Writing job involves assisting in the creation of scientific or medical documents, such as research papers, regulatory submissions, or educational materials, while working remotely. Interns typically conduct literature reviews, summarize clinical data, and ensure content adheres to medical guidelines. This role helps develop writing skills, industry knowledge, and experience in medical communication. It is ideal for students or recent graduates in life sciences, medicine, or pharmacy looking to gain hands-on exposure to medical writing.

What are the key skills and qualifications needed to thrive in the Internship Remote Medical Writing position, and why are they important?

To thrive as an Internship Remote Medical Writing professional, you need a solid understanding of life sciences or healthcare, excellent written communication skills, and attention to detail, often supported by relevant coursework or a related degree in progress. Familiarity with Microsoft Office, reference management software, and online collaboration platforms like Google Workspace is typically important, while certifications (such as GCP or relevant writing courses) are helpful but not always required. Strong time management, adaptability, and proactive communication distinguish top candidates in a remote team environment. These skills and qualifications are vital for delivering accurate, clear medical documents and collaborating effectively with editors and subject matter experts from a distance.

What kinds of projects or documents will I typically work on during a remote medical writing internship?

As a remote medical writing intern, you will generally assist with preparing clinical study summaries, regulatory documents, literature reviews, and content for medical education or marketing materials. Your daily tasks may include researching medical topics, editing and formatting documents, and collaborating with experienced writers or medical professionals for feedback and revisions. Working closely with your supervisor and team members via virtual meetings and shared drives is standard practice. This hands-on exposure helps you develop a strong foundation in medical writing conventions while building your professional portfolio.
What are the most commonly searched types of Remote Medical Writing jobs in Oregon? The most popular types of Remote Medical Writing jobs in Oregon are:
What are popular job titles related to Internship Remote Medical Writing jobs in Oregon? For Internship Remote Medical Writing jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Internship Remote Medical Writing jobs in Oregon look for? The top searched job categories for Internship Remote Medical Writing jobs in Oregon are:
What cities in Oregon are hiring for Internship Remote Medical Writing jobs? Cities in Oregon with the most Internship Remote Medical Writing job openings:
Infographic showing various Internship Remote Medical Writing job openings in Oregon as of May 2026, with employment types broken down into 14% Internship, 72% Full Time, and 14% Contract. Highlights an 100% Remote job distribution, with an average salary of $34,185 per year, or $16.4 per hour.
Manager, Medical Writing

Manager, Medical Writing

Danaher

On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Danaher rating

7.5

Company rating: 7.5 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

Within Danaher the work our diagnostic businesses do saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

We're accelerating the development of cutting-edge diagnostics to solve some of the world's most pressing health challenges. Across our diagnostics operating companies we are driving innovation through partnerships with top academic institutions and leading players in biopharma and translational research. We're bringing the best minds together to accelerate innovation and unlock the full potential of the latest scientific advances. Together, we're expanding access to precision diagnostics for millions of people worldwide - and we're using our unmatched global scale and proven playbook to make it happen, from hospital labs to mobile clinics. By helping providers, patients, and families get faster, more precise diagnostic results, we're improving treatment options and saving lives.

Learn about the Danaher Business System which makes everything possible.

The Manager, Medical Writing, is responsible for leading and developing the medical writing team for Danaher Diagnostics, overseeing the creation of high-quality clinical and regulatory documents for submission in the US and EU markets. You will manage a team of experienced medical writers, many with clinical backgrounds (MDs), ensuring scientific accuracy, regulatory compliance, and timely delivery of essential documentation to support clinical studies and product registrations.

This position within the Clinical Center of Excellence (CCOE) reports to the Senior Director, Clinical Compliance and Medical Writing, and will be fully remote.

In this role, you will have the opportunity to:

  • Lead, mentor, and performance manage a team of Medical Writers, providing guidance on document development, scientific content, and regulatory requirements for both US and EU submissions.
  • Oversee the planning, writing, editing, and quality control of a wide range of clinical and regulatory documents, including technical documentation for CE-IVDR/MDR, summaries, and responses to notified body questions, but also could include clinical study protocols, clinical study reports (CSRs), Investigator's Brochures (IBs), and similar documentation, as needed by the Clinical Development teams.
  • Ensure all medical writing activities and documents comply with Good Clinical Practice (GCP), relevant US (e.g., FDA) and EU (e.g., IVDR/MDR, EMA guidelines) regulatory guidelines, ICH guidelines, and company Standard Operating Procedures (SOPs).
  • Manage medical writing timelines and resources, ensuring timely delivery of high-quality documents to meet clinical study milestones and regulatory submission deadlines in both the US and EU.
  • Serve as a subject matter expert on medical writing best practices, document standards, for the US and EU.
  • Collaborate effectively with cross-functional teams including CCOE Clinical Development, Biostatistics, Data Management and Operating Company partners in Regulatory Affairs, Quality Assurance, Medical & Scientific Affairs and R&D to gather necessary input and ensure scientific accuracy and consistency across documents.
  • Implement continuous improvement to medical writing processes, templates, and standards to improve efficiency, consistency, and quality within the team, leading with DBS and leveraging AI in accordance with company policies.

The essential requirements of the job include:

  • Bachelor's degree in a scientific, medical, or related field with 7+ years' experience in medical writing within the pharmaceutical, biotechnology, diagnostics, or medical device industry, with significant experience preparing documents for US and EU regulatory submissions, or a Masters or Doctoral degree (MD, PhD, PharmD) with 4+ years of same experience.
  • 3+ years direct leadership experience managing a team of medical writers or other scientific/clinical professionals.
  • Demonstrated expert understanding of medical writing principles, styles, and standards (e.g., ICH guidelines, GCP).
  • Demonstrated strong knowledge of US FDA and EU regulatory requirements and guidance related to clinical and regulatory documentation (e.g., FDA guidance, IVDR/MDR requirements, EMA guidelines).
  • Experience working with clinical study data (including statistical output) and interpreting complex scientific and clinical information for inclusion in regulatory documents.
  • Proven ability to lead and develop a remote team of highly skilled professionals.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel <10%, as needed for DBS events and initiatives

It would be a plus if you also possess previous experience in:

  • Previous experience specifically in the diagnostics medical device industry preparing documentation requirements under IVDR.
  • Experience managing medical writers with advanced clinical degrees (e.g., MDs).
  • Experience with submission, review and publication of peer-reviewed journal articles.

Within Danaher Diagnostics, we offer a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

Within Danaher Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working within Danaher Diagnostics can provide.

The annual salary range for this role is $130-160k. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

#LI-LM3

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984