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Remote Medical Writer Jobs in Boston, MA (NOW HIRING)

Sigma Systems, Inc.

Medical Writer

Marlborough, MA · Remote

37554294 Remote Medical Writer, 7 Months Contract Sigma Systems is currently looking for a Remote Medical Writer The Medical Writer is responsible for authoring, reviewing, and coordinating the ...

New

YO AI Labs

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and ...

New

YO AI Labs

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and ...

New

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

Writes and/or contributes to abstracts and submissions of clinical data to various medical ... LI-remote About us With a firm belief that every person and community should have access to the ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

Writes and/or contributes to abstracts and submissions of clinical data to various medical ... LI-remote About us With a firm belief that every person and community should have access to the ...

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All JobsMedical Writer JobsRemote Medical Writer JobsRemote Medical Writer Jobs in Boston, MA

Remote Medical Writer information

See Boston, MA salary details

$15

$41

$62

How much do remote medical writer jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for remote medical writer in Boston, MA is $41.84, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $52.84 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 are the most commonly searched types of Medical Writer jobs in Boston, MA?

The most popular types of Medical Writer jobs in Boston, MA are:

What are popular job titles related to Remote Medical Writer jobs in Boston, MA?

For Remote Medical Writer jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Remote Medical Writer jobs in Boston, MA look for?

The top searched job categories for Remote Medical Writer jobs in Boston, MA are:

What cities near Boston, MA are hiring for Remote Medical Writer jobs?

Cities near Boston, MA with the most Remote Medical Writer job openings:

Remote Medical Writer jobs near you
Infographic showing various Remote Medical Writer job openings in Boston, MA as of August 2026, with employment types broken down into 65% Full Time, 15% Part Time, and 20% Contract. Highlights an 5% In-person, and 95% Remote job distribution, with an average salary of $87,037 per year, or $41.8 per hour.

Medical Writer

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

Posted yesterday

New

Job description

37554294 Remote Medical Writer, 7 Months Contract
Sigma Systems is currently looking for a Remote Medical Writer
The Medical Writer is responsible for authoring, reviewing, and coordinating the development of high-quality clinical and regulatory documents that support global clinical development programs. This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans

Responsibilities:

  • Author, edit, and review clinical and regulatory documents, including:
    • Clinical study protocols and protocol amendments
    • Investigator Brochures (IBs)
    • Clinical Study Reports (CSRs)
    • Briefing Book support
    • IND and NDA summary documents and other regulatory submission materials
  • Develop documents that are consistent with regulatory requirements, internal standards, and medical writing plans, while supporting the overall clinical development lifecycle and program objectives for one or more clinical development programs.
  • Collaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents.
  • Negotiate document deliverable milestones and timelines with cross-functional teams to ensure alignment across functions and adherence to medical writing plans and program objectives.
  • Facilitate document review cycles, resolve reviewer comments, and drive consensus among stakeholders while maintaining quality and schedule commitments.
  • Ensure documentation complies with applicable regulatory guidance, Good Clinical Practice (GCP), company standards, and industry best practices.
  • Contribute to the development and continuous improvement of medical writing processes, templates, style guides, and operational procedures.
  • Support regulatory submissions, health authority interactions, and inspection readiness activities as needed

Core Competencies

  • Scientific and regulatory writing expertise
  • Project and timeline management
  • Cross-functional collaboration and influence
  • Strategic thinking and problem solving
  • Attention to quality and regulatory compliance
  • Effective communication and stakeholder management

Requirements:

  • Advanced degree Bachelor's degree or more.
  • Experience authoring clinical and regulatory documents within the pharmaceutical, biotechnology, or clinical research industry.
  • Strong knowledge of clinical development, regulatory requirements, and applicable guidance documents (e.g., ICH guidelines).
  • Excellent scientific writing, editing, and communication skills.
  • Demonstrated ability to manage multiple projects and negotiate timelines in a cross-functional environment.

Strong organizational skills, attention to detail, and ability to work independently and collaboratively