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International Medical Writer Jobs (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 ... Knowledge of clinical operations, risk management, and international regulatory requirements.

Stryker

Senior Staff Medical Writer (Remote)

San Diego, CA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Knowledge of clinical operations, risk management, and international regulatory requirements.

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 ... Knowledge of clinical operations, risk management, and international regulatory requirements.

Stryker

Senior Staff Medical Writer (Remote)

Phoenix, AZ · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Knowledge of clinical operations, risk management, and international regulatory requirements.

Integrated Resources INC

Medical Writer

Raynham, MA · On-site

Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred. Expert ...

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 ... Knowledge of clinical operations, risk management, and international regulatory requirements.

Biodesix, Inc.

Medical Writer

$90K - $130K/yr

MEDICAL WRITER ABOUT US: Biodesix is a leading diagnostic solutions company, driven to improve ... Ensure all publications comply with Good Publication Practice (GPP), International Committee of ...

Stryker

Senior Staff Medical Writer (Remote)

Seattle, WA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Knowledge of clinical operations, risk management, and international regulatory requirements.

Telix Pharmaceuticals

Medical Writer

You will be supporting the international roll-out of our approved prostate cancer imaging agent and ... This role will provide medical writing support by organizing, analyzing, and interpreting ...

ApotheCom

Medical Writer

Yardley, PA · On-site +1

Medical Writer - Publications ApotheCom, an Inizio Medical company, is an exciting leader in the ... Working with leading international pharmaceutical clients, you will have the opportunity to ...

ApotheCom

Medical Writer

Yardley, PA · On-site

Medical Writer - Publications ApotheCom, an Inizio Medical company, is an exciting leader in the ... Working with leading international pharmaceutical clients, you will have the opportunity to ...

Veristat

Principal Medical Writer

Ontario, CA · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... International Council for Harmonisation (ICH) and other regulatory guidelines, and individual ...

Veristat

Principal Medical Writer

England, AR · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... International Council for Harmonisation (ICH) and other regulatory guidelines, and individual ...

Veristat

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... International Council for Harmonisation (ICH) and other regulatory guidelines, and individual ...

Veristat

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... International Council for Harmonisation (ICH) and other regulatory guidelines, and individual ...

Veristat

Principal Medical Writer

Scotland, PA · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... International Council for Harmonisation (ICH) and other regulatory guidelines, and individual ...

Veristat

Principal Medical Writer

Columbia, SC · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... International Council for Harmonisation (ICH) and other regulatory guidelines, and individual ...

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International Medical Writer information

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$14

$38

$57

How much do international medical writer jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for international medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What does an international medical writer do?

An International Medical Writer creates and manages medical documents for global healthcare audiences, including regulatory authorities, healthcare professionals, and patients. They write clinical study reports, regulatory submissions, scientific publications, and medical communications while ensuring compliance with international guidelines. This role requires strong scientific knowledge, attention to detail, and the ability to communicate complex medical information clearly. They often collaborate with cross-functional teams, including researchers, clinicians, and regulatory experts.

What does a typical workday look like for an international medical writer?

A typical day for an International Medical Writer involves researching scientific literature, drafting and editing regulatory or clinical documents, and collaborating virtually with cross-functional teams across different countries. You may participate in meetings with clients or internal stakeholders to clarify project requirements and timelines. Reviewing feedback, ensuring consistency with regional guidelines, and managing multiple assignments are also part of the routine. The role often requires balancing independent work with frequent communication and collaboration to ensure accuracy and timely project delivery.

What are the key skills and qualifications needed to thrive as an international medical writer?

To thrive as an International Medical Writer, a solid background in life sciences or medicine, exceptional written English, and familiarity with global regulatory guidelines are essential. Competence with tools such as Microsoft Office Suite, reference management software, and submission platforms like CTD/eCTD is often required; certification from organizations like AMWA or EMWA can be advantageous. Strong cross-cultural communication, attention to detail, and the ability to manage multiple projects under tight deadlines set top performers apart. These skills ensure the production of accurate, compliant medical documents that meet the diverse standards of international clients and regulatory bodies.

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What are the most commonly searched types of International Medical Writer jobs?

The most popular types of International Medical Writer jobs are:

What job categories do people searching International Medical Writer jobs look for?

The top searched job categories for International Medical Writer jobs are:

International Medical Writer jobs near you
Infographic showing various International Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Denver, CO • On-site, Remote

$143K - $238K/yr

Full-time

Posted 6 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 494 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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