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Full Time Remote Medical Writer Jobs (NOW HIRING)

GlaxoSmithKline

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

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 ...

BeiGene, Inc.

Principal Medical Writer

This position is also responsible for mentoring MWs (full-time employees and/or contractors/vendors ... medical writing communities). Supervisory Responsibilities: * None. Education Required: * An ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

Trilogy

Senior/Principal Medical Writer - USA

Durham, NC · On-site +1

$120K - $159K/yr

... remote) from our Durham, NC, USA office. You willbe responsible for: * Preparinga variety of ... As a Senior/Principal Medical Writer, you will: * Function as a lead writer to prepare a variety of ...

BeiGene, Inc.

Principal Medical Writer

$119K - $159K/yr

This position is also responsible for mentoring junior MWs (full-time employees and/or contractors ... and medical writing communities) with guidance from line manager/mentor. Supervisory ...

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Full Time Remote Medical Writer information

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$57

How much do full time remote medical writer jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for full time 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.

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

AspectFull Time Remote Medical WriterMedical Communications Specialist
CredentialsTypically requires a degree in life sciences, healthcare, or related field; certifications like AMWA or EMWA are commonSimilar credentials; often holds advanced degrees and certifications in medical writing or communication
Work EnvironmentPrimarily remote, working independently or with teams on scientific documentsCan be remote or in-office, involved in creating and managing medical communication materials
Industry UsageUsed across pharmaceutical, biotech, and healthcare industries for document preparationCommon in pharmaceutical marketing, medical education, and scientific publication sectors

While both roles require scientific expertise and similar credentials, Full Time Remote Medical Writers focus on creating scientific documents remotely, whereas Medical Communications Specialists often handle broader communication strategies, sometimes in a more collaborative or client-facing setting.

Can you work from home as a medical writer?

Full-time remote medical writers can work from home, as the role primarily involves researching, writing, and editing medical content using digital tools. Many employers offer remote positions with flexible schedules, provided the writer has strong communication skills and relevant certifications or experience. The ability to work independently and meet deadlines is essential for remote medical writing jobs.

How to make $100,000 a year working from home?

A full-time remote medical writer can earn $100,000 annually by gaining specialized knowledge in a high-demand medical field, building a strong portfolio, and working for reputable organizations or freelance clients. Developing skills in scientific writing, obtaining relevant certifications, and using professional tools like reference management software can enhance earning potential. Consistent quality work and expanding your network are key to reaching this income level remotely.

Is there a demand for medical writers?

The demand for medical writers remains strong due to the ongoing need for clear scientific communication in healthcare, pharmaceuticals, and regulatory industries. Full-time remote medical writers with expertise in scientific writing, regulatory guidelines, and familiarity with tools like EndNote or reference management software are sought after, especially as remote work becomes more prevalent.

How can I make 2000 a week working from home?

A full-time remote medical writer can earn $2,000 or more weekly by producing high-quality scientific or medical content, often charging per project or word. Building expertise, obtaining relevant certifications, and working with multiple clients or agencies can increase earning potential. Consistent, efficient work and strong research skills are essential for reaching this income level.
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What job categories do people searching Full Time Remote Medical Writer jobs look for? The top searched job categories for Full Time Remote Medical Writer jobs are:
Full Time Remote Medical Writer jobs near you
Infographic showing various Full Time Remote Medical Writer job openings in the United States as of July 2026, with employment types broken down into 74% Full Time, 24% Part Time, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Associate Director, Medical Writer

Associate Director, Medical Writer

MannKind Corporation

Westlake Village, CA • On-site, Remote

$148K - $222K/yr

Full-time

Posted 9 days ago

Job description

MannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions, developing and commercializing innovative inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases. The company applies deep expertise in formulation science and inhalation‑device engineering to reduce the treatment burden for conditions such as diabetes, congestive heart failure, pulmonary fibrosis, and pulmonary hypertension.

MannKind’s core technologies, including ultrafine dry‑powder formulations and advanced inhalation platforms, enable rapid, convenient delivery of medicines directly to the deep lung. This approach supports both local pulmonary targeting and systemic delivery for various medical indications. Through alternative drug formulations and delivery mechanisms, MannKind aims to bring forward differentiated, patient‑centric therapies that expand treatment options to improve outcomes across chronic and rare diseases.
At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Position Summary:
MannKind Corporation is seeking a detail-oriented and highly organized Medical Writer to join our team. The Medical Writer will provide advanced scientific writing expertise and ensure the successful preparation of high-quality documents including but not limited to study protocols, CSRs, DSURS, IB, safety narratives, publications and submission documents. This role involves providing medical writing support for multiple compounds and projects within multiple therapeutic areas, potentially interfacing with external groups, and serving as the scientific writing expert for the department.
Essential Duties and Job Functions:
  • Coordinate and lead the review, approval, and production of writing projects, arranging and driving review meetings with cross-functional teams.
  • Ensure effective communication among project team members and contributors, holding them accountable to agreed-upon project dates.
  • Leads strategic document preparation for INDs, NDAs and briefing documents
  • Establish best practices, workflow infrastructure/templates, and standards to enhance consistency and quality across all regulatory and scientific documents.
  • Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.
  • Stay abreast of global regulatory requirements and guidelines (FDA, EMA, PMDA, ICH, etc.), ensuring company compliance and best practices.
  • Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing.
  • Lead and oversee medical writing project timelines, ensuring alignment with broader corporate milestones.
  • Serve as the medical writer representative on project teams.
  • Write and edit scientific, clinical, or abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives.
  • Complete reviews, quality checks and approvals.
  • Summarize results presented in graphical, tabular, and/or listing format.
  • Interpret complex clinical data and convert it into clear, concise, and engaging scientific content for diverse audiences.
Knowledge, Experience and Skills:
  • BS/BA +12 / MS/MBA 8-10, PhD 5+
  • Degree in science or medical related field. Master’s or PhD preferred.
  • Minimum of 7 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R amp;D.
  • Knowledge of US and international regulations, requirements, and guidance associated with writing projects.
  • Excellent written and oral communication skills, attention to detail, and ability to correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy.
  • Extensive experience working with collaborative, cross-functional teams
  • Develop and/or update document templates, work instructions, style guides, and department-related processes (SOPs)
  • Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred.
  • Understanding of publication/scientific communication guidelines.
  • Ability to provide strategic oversight while managing multiple priorities in a fast-paced environment.
  • Deep understanding of ICH-GCP guidelines and other relevant regulatory requirements.
  • Strategic thinker with strong execution skills.
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