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Medical Writer Jobs (NOW HIRING)

Medasource

HEOR Medical Writer

Whippany, NJ · On-site +1

$30 - $40/hr

Medical Writer - Clinical Content & Health Economics and Outcomes Research (HEOR), Clinical Content Creation Group Location: Remote Duration: 6 month contract with the potential for extension, based ...

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Senior Medical Writer - Full-Time Remote Opportunity ───── Location: Fully Remote (U.S.) Industry: Pharmaceutical / Biotechnology Employment Type: Full-Time Salary Range: $142,100 - $195 ...

MJH Life Sciences

Medical Writer

Cranbury, NJ · On-site

$55K - $60K/yr

As a Medical Writer with the Enterprise Content Team at MJH Life Sciences ® , you will play a vital role in developing educational content for healthcare professional audiences. This position offers ...

Omnicom Health

Freelance Medical Writer

New York, NY · On-site

$90 - $130/hr

Freelance Medical Writer Healthcare Consultancy Group (HCG) is seeking a freelance medical writer with strong medical writing experience in a Medical Communications agency working on projects in ...

Intellectt INC

Medical Writer III

Maple Grove, MN · On-site

Medical Writer III Location:Maple Grove, MN - 55311 Key Responsibilities * Author and review CERs, CEPs, SSCPs, PMS/PMCF Plans & Reports, and other regulatory document * Analyze clinical data ...

Lumanity

Senior Medical Writer

Yardley, PA · Remote

The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical communications projects and deliverables including clinical publications (manuscripts and abstracts ...

Nucleus Global

Senior Medical Writer

Yardley, PA · On-site

Senior Medical Writer - Publications Nucleus Global is an exciting leader in the field of medical communications. Drawn together from several backgrounds including the pharmaceutical industry ...

Jj

Medical Writer III

Spring House, PA · On-site +1

Medical Writing Job Category: Professional All Job Posting Locations: Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania ...

New

Nucleus Global

Senior Medical Writer

Yardley, PA · On-site

Senior Medical Writer - Publications Nucleus Global is an exciting leader in the field of medical communications. Drawn together from several backgrounds including the pharmaceutical industry ...

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Medical Writer information

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How much do medical writer jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for 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.

Do you need a PhD to be a Medical Writer?

A PhD is not required to become a Medical Writer, but many professionals in the field hold advanced degrees such as a master's or doctorate. Strong writing skills, a background in life sciences or healthcare, and familiarity with scientific literature are essential for success in this role.

What are medical writers?

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.

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 involves working with scientific data, regulatory documents, and medical publications.

What Is the Job of a Medical Writer?

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 is a Medical Writer?

A medical writer is a professional who creates scientific and medical documents such as research articles, regulatory submissions, and clinical trial reports. They combine expertise in medicine or life sciences with strong writing skills to communicate complex information clearly and accurately, often working in pharmaceutical, biotech, or healthcare industries.

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

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.

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.

How do I become a Medical Writer?

To become a medical writer, typically a bachelor's degree in life sciences, healthcare, or a related field is required, often supplemented by advanced degrees or certifications in medical writing or regulatory writing. Gaining experience through internships, developing strong writing skills, and becoming familiar with industry guidelines and tools like reference management software can improve job prospects.

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.
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Medical Writer jobs near you
HEOR Medical Writer

HEOR Medical Writer

Medasource

Whippany, NJ • On-site, Remote

$30 - $40/hr

Contractor

Re-posted 5 hours ago

Job description

Medical Writer - Clinical Content & Health Economics and Outcomes Research (HEOR), Clinical Content Creation Group
Location: Remote
Duration: 6 month contract with the potential for extension, based on performance
Targeted compensation: $30-40/hr
Culture and Values
Our people are our strength-combining collaboration, speed, and quality while fostering a positive team culture and strong standardization to enable confident, compliant decision-making.
Purpose / Role Summary
The Medical Writer - Clinical & HEOR is responsible for developing high-quality, scientifically rigorous, compliant, and engaging content across clinical, medical, and HEOR domains. This role plays a critical role in shaping scientific and value-based narratives that support engagement with diverse stakeholders, including HCPs, payers, IDNs, and health systems. The position requires strong scientific and HEOR literacy, excellent writing skills, and the ability to translate complex clinical, economic, and outcomes data into clear, audience-appropriate materials aligned with therapeutic area and brand objectives.
Key Responsibilities
Scientific & Medical Content Development
• Author and support complex scientific deliverables including abstracts, posters, manuscripts, oral presentations, publication extenders, response documents, and white papers across therapeutic areas.
• Develop Medical Information content such as standard response letters, FAQs, and customer-facing materials.
• Draft, edit, and review HEOR-related outputs including value dossiers, slide decks, economic evidence materials, and submissions.
HEOR & Data Interpretation
• Conduct comprehensive literature searches and systematic or targeted reviews to support clinical and HEOR narratives.
• Partner with health economists, TA researchers, analysts, and statisticians to accurately interpret and translate data from clinical studies, real-world evidence, cost-effectiveness analyses, and budget impact models.
Publications & Congress Support
• Support preparation and submission of content for peer-reviewed journals and scientific congresses.
• Ensure adherence to publication standards and best practices (e.g., GPP, ICMJE, ISMPP) throughout the content lifecycle.
Compliance, Quality & Standards
• Ensure all materials comply with client policies and external regulatory and ethical guidelines (e.g., FDA/EMA, AMA style).
• Maintain high standards for accuracy, consistency, and scientific integrity across all deliverables.
Collaboration & Project Management
• Collaborate cross-functionally with internal creative, editorial, medical, and strategic partners.
• Manage multiple concurrent projects while meeting timelines, quality expectations, and stakeholder needs.
• Provide flexible writing support across group initiatives as priorities evolve.
Qualifications
Required
• PharmD or advanced scientific degree OR Bachelor's degree in life sciences, pharmacy, public health, health economics, or related field with relevant experience.
• 1-3+ years of experience in medical writing, medical communications, pharma, consultancy, or related environment; HEOR experience preferred.
• Strong scientific literacy with the ability to interpret and synthesize clinical, medical, and economic data.
• Excellent writing and editing skills tailored to both scientific and non-scientific audiences.
• Knowledge of clinical research processes, publication practices, and regulatory standards.
• Strong attention to detail, organization, and ability to work independently within cross-functional teams.
• Proficiency with standard authoring and reference tools (e.g., Microsoft Office, EndNote, Adobe Acrobat).
Preferred / Nice to Have
• Experience with HEOR methodologies (e.g., real-world evidence, cost-effectiveness analyses, budget impact models).
• Familiarity with publication and approval platforms (e.g., Veeva Vault, Pubstrat, iEnvision/Datavision, Nubela).
• Knowledge of AMA style and global publication guidelines.
• Professional certification (e.g., CMPP).
• Background working within a pharmaceutical company or healthcare consultancy.

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