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Medical Writer Work From Home Jobs (NOW HIRING)

BioMarin Pharmaceutical Inc.

Senior Medical Writer

Our success comes from our unwavering commitment to excellence, our deep understanding of patient ... Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful ...

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

... and work independently in a remote environment ───── Ideal Candidate Profile ───── Highly experienced clinical medical writer with strong Phase I-III study expertise Focused ...

Syneoshealth

Principal Medical Writer - Publications

OR · Remote

... to work with. Why? Because we know that when we bring together smart colleagues from across the ... Manages medical writing activities associated with individual studies, coordinating medical writing ...

Praxis Precision Medicines, Inc.

Senior Medical Writer

$130K - $150K/yr

... from the Associate Director, Medical Writing while also helping teams follow medical writing ... You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations ...

Lumanity

Senior Medical Writer

Yardley, PA · On-site +1

The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... work on multiple projects relating to multiple products in various therapeutic areas. Additional ...

Lumanity

Senior Medical Writer

Yardley, PA · Remote

The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... work on multiple projects relating to multiple products in various therapeutic areas. Additional ...

Lumanity

Senior Medical Writer

Yardley, PA · Remote

The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... work on multiple projects relating to multiple products in various therapeutic areas. Additional ...

Amiculum

Experienced medical writer - USA

Chicago, IL · On-site +1

Reviewing and providing constructive feedback on the work of other medical writers * Maintaining a ... If you require any adjustments or have specific needs, please contact Becka or Steven from our ...

Real Chemistry

Senior Medical Writer

The Senior Medical Writer serves as an integral part of the Real Chemistry Medical Communications ... work environment where our employees feel empowered to leverage all they bring from their personal ...

Syneoshealth

Medical Writer II - Publications

OR · Remote

Medical Writer II - Publications Syneos Health is a leading fully-integrated life sciences services ... to work with. Why? Because we know that when we bring together smart colleagues from across the ...

Precision for Medicine

Senior Medical Writer

$100K - $151K/yr

Ability to independently formulate key messages from clinical study data * Ability to author ... Ability to work effectively in a fast-paced environment with multiple high priority projects with ...

Precision Medicine Group

Senior Medical Writer

$100K - $151K/yr

Ability to independently formulate key messages from clinical study data * Ability to author ... Ability to work effectively in a fast-paced environment with multiple high priority projects with ...

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How much do medical writer work from home jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for medical writer work from home 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 are the key skills and qualifications needed to thrive as a Medical Writer working from home, and why are they important?

Medical Writers working from home need a strong background in life sciences, excellent writing skills, and typically a degree in a relevant scientific field. Familiarity with reference management tools, style guides like AMA or APA, and document collaboration platforms is important. Attention to detail, time management, and effective remote communication are crucial soft skills for this position. These competencies ensure accurate, clear, and timely medical content delivery while collaborating efficiently in a virtual environment.

How do remote medical writers typically collaborate with subject matter experts and regulatory teams?

Remote medical writers often use digital communication tools such as video conferencing, email, and project management platforms to collaborate closely with subject matter experts, researchers, and regulatory teams. Regular virtual meetings and document-sharing platforms facilitate timely feedback and ensure alignment on content accuracy and compliance with guidelines. Adapting to various communication styles and maintaining clear, organized documentation are essential for effective remote teamwork in this role.

What is the difference between Medical Writer Work From Home vs Medical Editor?

AspectMedical Writer Work From HomeMedical Editor
CredentialsTypically requires a degree in life sciences or related field, often with writing certificationsUsually holds a similar degree, with additional editing or proofreading certifications
Work EnvironmentRemote, independent work often with freelance or contract opportunitiesRemote or in-office, often employed by publishing or pharmaceutical companies
Industry UsageCommonly used in pharmaceutical, biotech, and healthcare communicationsUsed in publishing, medical journals, and regulatory documentation
Search & Comparison IntentOften compared for writing roles with flexible work optionsCompared for editing and quality control roles in medical content

Medical Writer Work From Home and Medical Editor roles share similar credentials and industry usage, but differ mainly in focus—writing versus editing. Medical writers create original content, while medical editors review and refine existing material. Both roles can be remote, but their primary tasks and skill sets distinguish them.

What does a Medical Writer who works from home do?

A Medical Writer working from home creates scientific documents, articles, regulatory submissions, and educational materials about healthcare topics. They research complex medical information and translate it into clear, accurate content for healthcare professionals, regulatory agencies, or the general public. Remote Medical Writers use digital tools to collaborate with other professionals and ensure their work meets industry standards and client requirements.

How to Become a Medical Writer Who Works From Home

To become a home-based medical writer, you can pursue a master’s degree in life sciences, though a bachelor’s degree in English with supplemented medical experience may be acceptable. Some medical writing positions require a doctorate in the field you write about and a background in research. In this role, you are expected to stay up-to-date on current findings in the medical field. Additional qualifications include familiarity with medical terminology, a firm grasp of grammar, editing skills, reliable internet access, and the ability to meet deadlines. Keen attention to detail and the ability to conduct research are also essential traits.

More about Medical Writer Work From Home jobs
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What states have the most Medical Writer Work From Home jobs? States with the most job openings for Medical Writer Work From Home jobs include:
What job categories do people searching Medical Writer Work From Home jobs look for? The top searched job categories for Medical Writer Work From Home jobs are:
Medical Writer Work From Home jobs near you
Senior Medical Writer

Senior Medical Writer

BioMarin Pharmaceutical Inc.

Remote

Full-time

Posted 4 days ago

Job description

Description
Who We Are:
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people's lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Worldwide Research and Development
From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.
ROLE:
The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications.
RESPONSIBILITIES:
  • Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
  • Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PBRERs, DSURs, etc.)
  • Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries).
  • Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
  • Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams).
  • Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met.
  • Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
  • Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
  • Adheres to departmental procedures and practices and technical and industry standards during all aspects of work.
  • Works effectively with cross-functional groups within BioMarin
  • Other tasks as assigned.

SCOPE:
  • This position progressively develops the medical writing function in alignment with the requirements of the Development Sciences department and organizational goals.
  • Filling this need with a regular full-time employee will enable BioMarin to reduce writing-related CRO and contractor costs, increase Global Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications.

EXPERIENCE:
  • Up to 6 years of as a medical writer in the pharmaceutical industry - OR - at least 10 years of medical or scientific writing experience as a primary job responsibility.

1) Medical Writing:
  • Experience writing, reviewing, or editing protocols and clinical study reports required.
  • Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred.
  • Experience writing, reviewing, or editing regulatory briefing books preferred.
  • Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content.
  • Ability to interpret and create complex tabular and graphical clinical data presentations.
  • Advanced applied knowledge of basic clinical laboratory tests.
  • Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug).
  • 2) Clinical Studies
  • Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets.
  • Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection.
  • Intermediate to advanced applied knowledge of:

o documentation required for the conduct of clinical studies
o protocol design (including objectives, efficacy and safety endpoints, and procedures for collecting and reporting AEs and SAEs)
o study results reporting
o integrated results reporting
  • Direct experience with documentation in all phases of drug development.
  • 3) Regulatory
  • Intermediate to advanced knowledge of regulatory requirements and guidances associated with standalone regulatory documents (eg, protocols, investigator brochures, and clinical study reports).
  • Prior familiarity with standard eCTD IND/NDA work, including:

o Modules 2, 3, 4, and 5 of INDs/NDAs in eCTD format
o Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE)
  • 4) Project Management
  • Capable of working on multiple tasks and shifting priorities.
  • Capable of leading a cross-functional team under strict timelines, including calling/running meetings and managing team review and comment adjudication stages of document preparation.
  • Capable of representing Global Medical Writing at cross-functional meetings, advocating for Global Medical Writing, and working with Global Medical Writing line management to resolve cross-functional conflicts.
  • Good conflict management skills.
  • Motivated and shows initiative.
  • Detail oriented.
  • 5) Communication
  • Capable of well organized, concise and clear written and verbal communication.
  • Capable of comprehending complex scientific concepts and translating them into clear, concise, appropriately referenced text that meets regulatory requirements.
  • Effective at explaining writing principles to a varied audience both in individual and group settings; intermediate to advanced presentation skills.

EDUCATION:
  • Bachelor's or higher degree required; scientific focus desirable.
    • Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association.

COMPUTER SKILLS:
  • Proficient in Microsoft Word (including the use of templates), Excel, Adobe Acrobat, MS Project/Project Server, and PowerPoint.
  • Experience using document management software (eg, LiveLink, SharePoint, Veeva)
  • Experienced with scanners, printers, and copiers.

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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