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Remote Medical Writer Jobs (NOW HIRING)

Argenx

Senior Medical Writer

$104K - $143K/yr

For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory ...

Revolution Medicines

Principal Medical Writer

$201K - $251K/yr

Serves as medical writing lead on complex clinical regulatory documents, including protocols, IBs, CSRs, briefing documents, periodic safety reports, risk management documents, and IND and NDA ...

Medtronic

Senior Medical Writer

North Haven, CT · On-site +1

This remote position offers the opportunity to collaborate daily with cross-functional partners ... Experience with medical and/or scientific writing within a medical device industry or related ...

Veristat

The Principal Medical Writer independently plans and prepares a range of regulatory documents and ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...

Real Chemistry

Senior Medical Writer

The Senior Medical Writer serves as an integral part of the Real Chemistry Medical Communications ... Some positions offer hybrid or remote flexibility, while others require regular in-office presence.

Medtronic

Senior Medical Writer

North Haven, CT · On-site +1

This remote position offers the opportunity to collaborate daily with cross-functional partners ... Experience with medical and/or scientific writing within a medical device industry or related ...

Medtronic

Senior Medical Writer

North Haven, CT · On-site +1

This remote position offers the opportunity to collaborate daily with cross-functional partners ... Experience with medical and/or scientific writing within a medical device industry or related ...

Parexel

Senior Medical Writer - FSP

Parexel FSP has an exciting opportunity for a Medical Writer ! Key Accountabilities : Author Clinical Documents * Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and ...

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Remote Medical Writer information

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$14

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How much do remote medical writer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for remote 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.

Is there a demand for remote medical writers?

There is a strong and growing demand for remote medical writers due to the increasing need for clear scientific communication in healthcare, pharmaceuticals, and biotech industries. Remote medical writing roles often require expertise in scientific writing, regulatory knowledge, and familiarity with tools like reference management software, making it a viable and expanding career option.

What is the difference between Remote Medical Writer vs Medical Communications Specialist?

AspectRemote Medical WriterMedical Communications Specialist
Required CredentialsTypically requires a degree in life sciences, healthcare, or related field; often a medical or scientific writing certificationSimilar credentials; may also require training in medical communication or marketing
Work EnvironmentPrimarily remote, working independently on scientific documentsOften collaborative, working with teams on strategic communication projects
Employer & Industry UsagePharmaceutical, biotech, and healthcare companies; contract agenciesPharmaceutical companies, medical education agencies, and healthcare marketing firms
Common Search & Comparison IntentYesYes

Remote Medical Writers focus on creating scientific documents independently, often remotely, while Medical Communications Specialists typically work in teams to develop broader communication strategies. Both roles require similar scientific backgrounds and are prevalent in healthcare industries, but their daily tasks and collaboration levels differ.

How do remote medical writers typically collaborate with subject matter experts and project teams while working offsite?

Remote Medical Writers often work closely with physicians, researchers, and regulatory professionals through virtual meetings, emails, and collaborative document platforms. Regular communication is essential to clarify scientific content, gather feedback, and ensure accuracy in documentation. Tools like Microsoft Teams, Zoom, and cloud-based editing platforms facilitate real-time collaboration and version control. Building strong working relationships and maintaining proactive communication are key to overcoming the challenges of remote teamwork in this role.

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

To thrive as a Remote Medical Writer, you need strong scientific knowledge, excellent writing skills, and a relevant degree in life sciences or medicine. Familiarity with referencing software, document management systems, and guidelines like ICMJE or AMA is typically required, along with experience using tools such as EndNote or PubMed. Attention to detail, time management, and the ability to communicate complex information clearly are standout soft skills for this role. These abilities are essential for producing accurate, credible, and timely medical content that meets regulatory and publication standards.

Can you work from home as a remote medical writer?

Yes, remote medical writers typically work from home or other remote locations, utilizing skills in scientific writing, research, and communication. They often use tools like document management software and may need to meet deadlines and quality standards set by employers or clients.

What is a remote medical writer?

Remote medical writers are professionals who create scientific documents, such as clinical study reports, regulatory submissions, medical articles, and educational materials, while working from a location outside of a traditional office setting. They typically have expertise in medical science and strong writing skills, enabling them to communicate complex medical information clearly and accurately. Remote medical writers often collaborate with healthcare professionals, researchers, and pharmaceutical companies using digital tools. Their work is crucial for ensuring that medical content is accurate, compliant with regulations, and accessible to its target audience. This role allows for location flexibility and is increasingly in demand within the healthcare and pharmaceutical industries.

What does a remote medical writer do?

As a remote medical writer, your duties are to work from home and write documents or articles for medical journals, promotional materials, and reports. In this position, you may collect medical information from clinical studies, examine the protocols used in those studies, and edit documents to ensure the clarity and consistency of the content. Most medical writers specialize in a particular type of content, such as writing research proposals or filling out paperwork for regulatory submissions. Although this is a remote position, companies tend to prefer applicants who are located in the same part of the country to make it easier to coordinate schedules and answer questions as needed.

More about Remote Medical Writer jobs
What cities are hiring for Remote Medical Writer jobs? Cities with the most Remote Medical Writer job openings:
What are the most commonly searched types of Medical Writer jobs? The most popular types of Medical Writer jobs are:
What states have the most Remote Medical Writer jobs? States with the most job openings for Remote Medical Writer jobs include:
What job categories do people searching Remote Medical Writer jobs look for? The top searched job categories for Remote Medical Writer jobs are:
Remote Medical Writer jobs near you
Infographic showing various Remote Medical Writer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, and 7% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Senior Medical Writer

Argenx

Remote

$104K - $143K/yr

Full-time

Medical, Retirement

Re-posted 23 hours ago

Job description

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.
We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.
For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory submissions.
This individual will execute the overall strategy for all medical writing processes according to argenx medical writing standards and corporate objectives.
Key Accountabilities/Responsibilities:
  • Author and project manage SME contribution to develop content for regulatory submissions that is well-organized, consistent, accurate, and compliant with argenx Medical Writing standards, including style guide, lexicon, templates, and libraries
  • Authors content for phase 1-4 protocols, master ICFs, IBs, and CSRs
  • Responsible for inspection-readiness of medical writing activities
  • Supports the lead writer and project teams to ensure project deadlines are met
  • Executes corporate objectives, goals, measures, and strategies
  • Capable of working on multiple deliverables simultaneously

Desired Skills and Experience:
  • Bachelor's degree in a scientific or clinical discipline or related field is required; Ph.D. preferred
  • Minimum of 3 years of related, sponsor-level pharma or biotech clinical/regulatory medical writing experience required; CRO experience considered
  • Native/bilingual or fluent American English proficiency
  • Solution-focused
  • Experience with Veeva Vault and Please Review
  • Experience with implementing lean writing techniques
  • Basic understanding of scientific methodology as applied to drug development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission
  • Familiarity with pharmacovigilance guidelines and developing aggregate reports
  • Ability to work precisely according to procedures and regulations
  • Ability to prioritize and multi-task successfully in a fast-paced environment
  • Ability to work autonomously, as well as in a team
  • Excellent written and verbal communication skills
  • Excellent time management skills and a proven ability to work on multiple projects at any given time
  • Must be proficient in MS Office

For applicants in the United States: The annual base salary hiring range for this position is $104,000.00 - $143,000.00 USD. This range reflects our good faith estimate at the time of posting. Individual compensation is determined using objective, inclusive, and job-related criteria such as relevant experience, skills, demonstrated competencies and internal equity. This means actual pay may differ from the posted range when justified by these factors. Because market conditions evolve, pay ranges are reviewed regularly and may be adjusted to remain aligned with external benchmarks.
This job is eligible to participate in our short-term and long-term incentive programs, subject to the terms and conditions of those plans and applicable policies. It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines.
At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.
Before you submit your application, CV or any other personal details to us, please review our argenx Privacy Notice for Job Applicants to learn more about how argenx B.V. and its affiliates ("argenx") will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at privacy@argenx.com.
If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@argenx.com. Only inquiries related to an accommodation request will receive a response.

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