Remote Medical Writer Jobs in United States

53 Medical Writer jobs in United States available for remote work from home. Apply for positions such as Medical Writer, Medical Writer, Medical Writer and more! Discover the best work-from-home or hybrid, full- and part-time jobs.

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Remote Medical Writer Jobs in United States (53)

Search = Medical Writer Remote in = United States

Medical Writer

Nucleus Global · Full Time · 3 Days Ago
Nucleus Global
๐ŸŒŽ United States โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
Lead the development of high-quality scientific written materials and innovative medical communications projects. Review and interpret preclinical and clinical research data to create content for physician and consumer audiences.
Systimmune is hiring for remote Medical Writer

Medical Writer

Systimmune · Full Time · 1 Week Ago
Systimmune
๐ŸŒŽ United States ๐Ÿ’ต $80000 - $130K per year โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
The medical writer manages and oversees the production of high-quality clinical documentation, including protocols, reports, and regulatory briefing materials. They ensure all documents meet scientific accuracy, regulatory guidelines, and established templates for submission to authorities.

Medical Writer

Verisk · Full Time · 1 Week Ago
Verisk
๐ŸŒŽ United States ๐Ÿ’ต $55000 - $57000 per year โญ 0-2 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Medical Writer reviews medical records to draft narrative summaries for Medicare Set Asides and Medical Cost Projections. They ensure all documentation is accurate and consistent with client protocols and internal guidelines.

Medical Writer

Orthofix · Full Time · 3 Weeks Ago
Orthofix
๐ŸŒŽ United States โญ 0-2 yrs exp ๐Ÿ’ผ Writing Medical Writer
The role involves writing and updating Clinical Evaluation Reports (CERs), PMCF reports, and SSCPs to comply with international regulations. It also requires analyzing clinical data and collaborating with cross-functional partners to respond to regulatory agency requests.

Medical Writer

Telix Pharmaceuticals (AMER) · Full Time · 7 Weeks Ago
Telix Pharmaceuticals (AMER)
๐ŸŒŽ United States โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
Lead the planning, writing, and editing of high-quality regulatory documents including CSRs, IBs, and eCTD summaries for clinical drug development. Collaborate with cross-functional teams to analyze scientific data and respond to health authority requests.

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Senior Medical Writer

Nucleus Global · Full Time · 2 Days Ago
Nucleus Global
๐ŸŒŽ United States โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Senior Medical Writer leads the development of high-quality scientific materials and innovative medical communications projects. Responsibilities include interpreting clinical research data, conducting literature searches, and synthesizing trial data for physician and consumer audiences.

Senior Strategic Medical Writer - Remote

AbbVie · Full Time · 4 Days Ago
AbbVie
๐ŸŒŽ United States ๐Ÿ’ต $96500 - $183K per year โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
Lead the preparation and writing of clinical and regulatory documents for drug and device development. Coordinate reviews and quality control processes to ensure compliance and timely delivery of submission objectives.
Veristat is hiring for remote Senior Medical Writer- Clinical Focus

Senior Medical Writer- Clinical Focus

Veristat · Full Time · 4 Days Ago
Veristat
๐ŸŒŽ Canada, United States ๐Ÿ’ต $116K - $128K per year โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Senior Medical Writer leads the authorship of clinical regulatory documents and manages smaller projects while supporting larger engagements. They interface directly with clients to ensure goals are met and maintain professional business relationships.
Veristat is hiring for remote Senior Medical Writer - Safety Focus

Senior Medical Writer - Safety Focus

Veristat · Full Time · 5 Days Ago
Veristat
๐ŸŒŽ Canada, United States ๐Ÿ’ต $116K - $128K per year โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
The role involves authoring various aggregate safety reports and serving as a project lead for smaller engagements. The writer will interface directly with clients and collaborate with larger delivery teams on complex projects.
Thermo Fisher Scientific is hiring for remote Senior Regulatory Medical Writer, Client-embedded, FSP

Senior Regulatory Medical Writer, Client-embedded, FSP

Thermo Fisher Scientific · Full Time · 1 Week Ago
Thermo Fisher Scientific
๐ŸŒŽ United States ๐Ÿ’ต $110K - $125K per year โญ 5-10 yrs exp ๐Ÿ’ผ Legal Medical Writer
The Senior Medical Writer authors routine and complex clinical regulatory documents, including study reports, protocols, and INDs. They collaborate with cross-functional teams to ensure document accuracy and mentor junior medical writers to maintain high-quality deliverables.
Thermo Fisher Scientific is hiring for remote Senior Medical Writer - Medical Information

Senior Medical Writer - Medical Information

Thermo Fisher Scientific · Full Time · 1 Week Ago
Thermo Fisher Scientific
๐ŸŒŽ United States โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Senior Medical Writer creates high-quality medical information documents, publications, and clinical study documents for internal and external clients. They are also responsible for reviewing team deliverables, mentoring new hires, and potentially assisting with program management activities.

Principal Medical Writer

MJH Life Sciencesยฎ · Full Time · 1 Week Ago
MJH Life Sciencesยฎ
๐ŸŒŽ United States ๐Ÿ’ต $95000 - $105K per year โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Principal Medical Writer will lead the development of high-quality scientific content across various therapeutic areas and ensure compliance with industry standards. Responsibilities include conducting literature reviews, managing writers, and preparing materials for promotional review processes.

Associate Director, Medical Writer

MannKind Corporation · Full Time · 2 Weeks Ago
MannKind Corporation
๐ŸŒŽ United States ๐Ÿ’ต $148K - $222K per year โญ 10+ yrs exp ๐Ÿ’ผ Writing Medical Writer
Lead the preparation and production of high-quality, ICH-compliant regulatory and scientific documents including protocols, CSRs, and IB. Coordinate cross-functional reviews and provide strategic medical writing oversight for multiple compounds across various therapeutic areas.

Senior Medical Writer

Ashfield MedComms · Full Time · 2 Weeks Ago
Ashfield MedComms
๐ŸŒŽ United States โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Senior Medical Writer develops high-quality scientific content, including manuscripts and congress materials, based on preclinical and clinical research data. They lead projects, interact with pharmaceutical clients, and provide editorial feedback to team members.
Red Nucleus is hiring for remote Senior Medical Writer (Medical Affairs)

Senior Medical Writer (Medical Affairs)

Red Nucleus · Full Time · 2 Weeks Ago
Red Nucleus
๐ŸŒŽ United States โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Senior Medical Writer leads the development and scientific integrity of medical content for pharmaceutical and medical device clients. This includes conducting literature research, creating scientific copy, and collaborating with cross-functional teams to ensure regulatory compliance.
Syneos Health is hiring for remote Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
๐ŸŒŽ United States ๐Ÿ’ต $95000 - $210K per year โญ 5-10 yrs exp ๐Ÿ’ผ Legal Medical Writer
Responsible for developing high-quality clinical regulatory documents for global submissions, including ISE, ISS, and Clinical Overviews. Provides strategic direction to cross-functional teams and mentors junior medical writers to ensure scientific rigor and regulatory compliance.

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Senior Medical Writer (Remote - US)

MMS · Full Time · 2 Weeks Ago
MMS
๐ŸŒŽ United States โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
The Senior Medical Writer is responsible for authoring and editing complex clinical development documents, including protocols and regulatory summaries. They must manage project timelines, coordinate directly with clients, and mentor junior medical writers.

Principal Medical Writer

ICON plc · Full Time · 3 Weeks Ago
ICON plc
๐ŸŒŽ Germany, United States โญ 10+ yrs exp ๐Ÿ’ผ Writing Medical Writer
Lead the development of high-quality regulatory and clinical documents, including clinical study reports and protocols. Oversee medical writing workstreams and mentor junior writers to ensure adherence to industry standards and timelines.
Syneos Health is hiring for remote Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
๐ŸŒŽ United States ๐Ÿ’ต $95000 - $210K per year โญ 10+ yrs exp ๐Ÿ’ผ Legal Medical Writer
Develop global regulatory submission documents including Clinical Study Reports and Clinical Overviews in accordance with ICH guidelines. Manage medical writing projects by developing timelines and coordinating with cross-functional teams to meet corporate objectives.
Amiculum is hiring for remote Experienced medical writer โ€“ USA

Experienced medical writer โ€“ USA

Amiculum · Full Time · 3 Weeks Ago
Amiculum
๐ŸŒŽ United States โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
Develop and deliver high-quality scientific content, including abstracts, posters, and manuscripts, for a global publications account. Build long-term client relationships and identify opportunities for organic growth within the oncology and hematology therapy areas.
BeiGene is hiring for remote Senior Principal Medical Writer

Senior Principal Medical Writer

BeiGene · Full Time · 3 Weeks Ago
BeiGene
๐ŸŒŽ United States ๐Ÿ’ต $137K - $182K per year โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
Responsible for developing high-quality clinical and regulatory documents to support the development and approval of products in the company pipeline. This role also involves mentoring other medical writers and leading process optimization for departmental tools and templates.

Contract Medical Writer - Remote

Sorcero · Full Time · 4 Weeks Ago
Sorcero
๐ŸŒŽ United States ๐Ÿ’ต $35 - $60 per hour โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
Review and develop AI-drafted manuscripts for pharmaceutical clients to ensure high-quality clinical trial publications. Liaise with authors to move manuscripts toward submission while adhering to strict confidentiality and data privacy parameters.
BeiGene is hiring for remote Senior Principal Medical Writer

Senior Principal Medical Writer

BeiGene · Full Time · 4 Weeks Ago
BeiGene
๐ŸŒŽ United States ๐Ÿ’ต $137K - $182K per year โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
Responsible for developing high-quality clinical and regulatory documents to support the development and approval of products in the oncology pipeline. This role also involves mentoring other medical writers and leading the optimization of departmental processes and templates.
BeiGene is hiring for remote Principal Medical Writer

Principal Medical Writer

BeiGene · Full Time · 4 Weeks Ago
BeiGene
๐ŸŒŽ United States ๐Ÿ’ต $119K - $159K per year โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
Responsible for developing high-quality clinical and regulatory documents to support the development and approval of products in the oncology pipeline. This role involves leading document strategy, managing timelines for complex submissions, and mentoring junior medical writers.

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Medical Writer I - Medical Imaging

ICON plc · Full Time · 5 Weeks Ago
ICON plc
๐ŸŒŽ United States โญ 2-5 yrs exp ๐Ÿ’ผ Writing Medical Writer
The role involves preparing high-quality medical imaging documentation, such as Site Imaging Manuals and Review Charters, to support clinical trials and regulatory submissions. The writer will collaborate with internal teams and sponsors to ensure accurate image acquisition and assessment criteria.

Senior Medical Writer

Precision Medicine Group · Full Time · 5 Weeks Ago
Precision Medicine Group
๐ŸŒŽ United States ๐Ÿ’ต $100K - $151K per year โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
Lead the development of high-quality clinical study documents, including protocols, IBs, and CSRs, ensuring compliance with regulatory guidelines. Manage the document lifecycle from template to final approval in collaboration with sponsors and internal teams.

Senior Medical Writer

Precision for Medicine · Full Time · 5 Weeks Ago
Precision for Medicine
๐ŸŒŽ United States ๐Ÿ’ต $100K - $151K per year โญ 5-10 yrs exp ๐Ÿ’ผ Writing Medical Writer
Lead the development of high-quality clinical study documents, including protocols, IBs, and CSRs, ensuring compliance with regulatory guidelines. Manage the document lifecycle from template to final approval in collaboration with sponsors and internal teams.

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