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Remote Senior 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 ...

Synchrony Group

Senior Medical Writer

West Chester, PA · On-site +1

The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...

Veristat

The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...

Veristat

The Senior Medical Writer - Safety Focus is a major contributor to document authorship for a ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...

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Remote Senior Medical Writer information

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$247.5K

How much do remote senior medical writer jobs pay per year?

As of Jul 23, 2026, the average yearly pay for remote senior medical writer in the United States is $137,286.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $166,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Senior Medical Writer, and why are they important?

A Remote Senior Medical Writer needs advanced scientific or medical knowledge, strong writing skills, and typically a relevant degree (e.g., life sciences, pharmacy, or medicine) with proven experience in medical communications. Familiarity with reference management tools, document management systems, and publication guidelines (such as ICMJE or GPP) is crucial. Exceptional attention to detail, time management, and the ability to communicate complex information clearly are standout soft skills. These competencies ensure the accurate, compliant, and timely delivery of high-quality medical documents vital for regulatory submissions, publications, and healthcare communications.

How does a Remote Senior Medical Writer typically collaborate with cross-functional teams while working off-site?

As a Remote Senior Medical Writer, you will regularly collaborate with medical, regulatory, and project management teams using virtual communication tools like video meetings, shared document platforms, and project management software. Clear and proactive communication is crucial, as you may need to bridge time zones and coordinate feedback from multiple stakeholders. While working remotely offers flexibility, it also requires strong organizational skills to manage deadlines and ensure your deliverables align with team objectives. Building strong relationships and maintaining transparency with your colleagues are key to ensuring smooth project progression and high-quality medical content.

What is the difference between Remote Senior Medical Writer vs Remote Medical Writer?

AspectRemote Senior Medical WriterRemote Medical Writer
CredentialsTypically requires advanced degrees (MD, PhD, PharmD) and experienceOften requires a relevant degree, such as life sciences or healthcare, with less experience needed
Work EnvironmentWorks independently or leads projects, often in a collaborative team settingSupports medical writing tasks under supervision, often in a team
Employer & Industry UsageUsed by pharmaceutical, biotech, and healthcare companies for complex documentationUsed across similar industries for standard medical content creation

The main difference between a Remote Senior Medical Writer and a Remote Medical Writer lies in experience, responsibilities, and credentials. Senior Medical Writers typically have advanced degrees and more experience, handling complex projects and leading teams. Medical Writers are often earlier in their careers, focusing on supporting documentation tasks under supervision. Both roles are vital in the healthcare and pharmaceutical industries, but the senior position involves greater expertise and leadership responsibilities.

What are remote senior medical writers?

Remote senior medical writers are experienced professionals who create, review, and edit scientific and medical documents for pharmaceutical, biotechnology, or healthcare organizations while working from a remote location. Their work includes regulatory documents, clinical study reports, manuscripts, and educational materials. They ensure complex medical information is communicated clearly and accurately for both professional and lay audiences, and often collaborate with scientists, physicians, and regulatory teams. Senior medical writers typically have advanced degrees in life sciences and several years of writing experience.
More about Remote Senior Medical Writer jobs
What cities are hiring for Remote Senior Medical Writer jobs? Cities with the most Remote Senior Medical Writer job openings:
What are the most commonly searched types of Senior Medical Writer jobs? The most popular types of Senior Medical Writer jobs are:
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Remote Senior Medical Writer jobs near you
Infographic showing various Remote Senior 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 $137,286 per year, or $66 per hour.
Senior Medical Writer

Senior Medical Writer

BioMarin Pharmaceutical Inc.

Remote

Full-time

Posted 16 days ago

BioMarin Pharmaceutical rating

8.3

Company rating: 8.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

20th of 74 rated pharmaceutical

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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