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Medical Writer Jobs in Boston, MA (NOW HIRING)

Medical Writer

Boston, MA ยท On-site

$55 - $70/hr

Medical Writing Science Manager ๐Ÿ“ Boston, MA | Hybrid -- 3 days onsite / 2 days remote ๐Ÿ’ผ Initial 2-month contract | Potential for extension or conversion ๐Ÿ’ฐ $55-$70/hour โฐ 40 hours/week We ...

Medical Writer - Remote

Boston, MA ยท On-site

$50 - $80/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 ...

Medical Writer - Remote

Boston, MA ยท 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 ...

Medical Writer - Remote

Boston, MA ยท 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 ...

Analyst/Medical Writer

Boston, MA ยท On-site

$71K - $76K/yr

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...

Analyst/Medical Writer

Boston, MA ยท On-site

$71K - $76K/yr

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...

Senior Medical Writer

Boston, MA ยท On-site

$90K - $100K/yr

Senior Medical Writers take a leading role across projects, providing strategic advice to clients, supervising the project team, and producing high-quality scientific content themselves. They ensure ...

Analyst/Medical Writer

Boston, MA ยท Hybrid

$71K - $76K/yr

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...

Senior Medical Writer

Boston, MA ยท On-site

$90K - $100K/yr

Senior Medical Writers take a leading role across projects, providing strategic advice to clients, supervising the project team, and producing high-quality scientific content themselves. They ensure ...

Senior Medical Writer

Boston, MA ยท Hybrid

$90K - $100K/yr

Senior Medical Writers take a leading role across projects, providing strategic advice to clients, supervising the project team, and producing high-quality scientific content themselves. They ensure ...

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Medical Writer information

See Boston, MA salary details

$12

$50

$85

How much do medical writer jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for medical writer in Boston, MA is $50.26, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $60.87 per hour, depending on experience, location, and employer.

What is a medical writer?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

What does a medical writer do?

Medical writers create scientific documents and articles. This can include a variety of different types of papers, including research documents, educational or promotional literature, articles, and abstracts. You may ghostwrite for well-known physicians and scientists, or you may write under your own name, depending on what field you are in. Other medical writer jobs include journalists for medical magazines, authors of books, and those who write marketing materials for health care organizations. Regardless of your specialty, you must be able to interpret complex scientific information and create articles that people can read and understand, particularly when writing for the general public.

What skills and qualifications are needed to be a medical writer?

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

How does a medical writer typically collaborate with subject matter experts during a project?

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals can earn over $100,000, especially with specialized knowledge or certifications. The role often requires strong writing skills and familiarity with scientific or medical terminology.

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 Medical Writer jobs in Boston, MA?

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

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

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

Infographic showing various Medical Writer job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $104,545 per year, or $50.3 per hour.

$55 - $70/hr

Other

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Medical Writing Science Manager


๐Ÿ“ Boston, MA | Hybrid โ€” 3 days onsite / 2 days remote

๐Ÿ’ผ Initial 2-month contract | Potential for extension or conversion

๐Ÿ’ฐ $55โ€“$70/hour

โฐ 40 hours/week


We are seeking a Medical Writing Science Manager to join a collaborative clinical development team supporting the preparation of high-quality clinical and regulatory documents.

This is a highly cross-functional opportunity for a scientific professional with strong clinical knowledge and writing skills who can analyze complex clinical and non-clinical information, identify key messages, and translate years of research data into clear, concise, scientifically accurate documents.


What Youโ€™ll Do

  • Author moderately complex clinical and regulatory documents in collaboration with Clinical Development, Medical, Regulatory, Biostatistics, and other cross-functional partners.
  • Serve as the Medical Writing lead for moderately complex clinical studies.
  • Support clinical teams with the review and interpretation of study data and help address questions related to study results and documentation.
  • Develop clear, concise key messages and scientific narratives for clinical and regulatory documents.
  • Analyze and synthesize clinical and non-clinical data from multiple sources to develop accurate, audience-appropriate documents.
  • Ensure consistency of medical and scientific information across related documents and studies within a clinical program.
  • Contribute scientific and clinical expertise to clinical development plans and other program-level documents.
  • Coordinate input from multiple stakeholders and manage document development timelines and deliverables.
  • Participate in process improvements and development of procedures related to Medical Writing.
  • Apply strong project management and organizational skills to manage multiple priorities in a fast-paced, cross-functional environment.


Key Qualifications

  • Ph.D. or equivalent advanced degree in a relevant scientific or clinical discipline.
  • Approximately 4+ years of relevant experience in medical writing, clinical research, drug development, or a related field.
  • Demonstrated experience writing and editing clinical and regulatory documents.
  • Strong clinical knowledge and understanding of clinical development and clinical research.
  • Ability to analyze, interpret, and summarize complex clinical and scientific data.
  • Experience translating extensive research data into clear, concise, and scientifically rigorous documents.
  • Experience with clinical regulatory documents such as:
  • Clinical Study Reports (CSRs)
  • Clinical study protocols
  • Investigator's Brochures (IBs)
  • Regulatory submission documents
  • Broad understanding of drug development, study design, biostatistics, pharmacology, regulatory requirements, and medical terminology.
  • Excellent written and verbal communication skills.
  • Strong collaboration and stakeholder-management skills, with the ability to work effectively across multiple functions.
  • Strong project management, organization, and prioritization skills.
  • Ability to work independently, identify solutions, and manage competing priorities with appropriate guidance.