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Consultant Medical Writer Jobs (NOW HIRING)

Medical Writer - Remote

Atlanta, GA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Boston, MA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Los Angeles, CA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Palo Alto, CA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Austin, TX ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

New York, NY ยท Remote

$50 - $80/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Phoenix, AZ ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Philadelphia, PA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Seattle, WA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

Medical Writer - Remote

Seattle, WA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

Medical Writer - Remote

Chicago, IL ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Houston, TX ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Dallas, TX ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Washington, DC ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

Medical Writer - Remote

Miami, FL ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

Boston, MA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

New

Medical Writer - Remote

San Jose, CA ยท Remote

$50 - $90/hr

Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...

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Consultant Medical Writer information

See salary details

$11

$46

$78

How much do consultant medical writer jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for consultant medical writer in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

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

As a Consultant Medical Writer, effective collaboration with clients and subject matter experts (SMEs) is essential for producing accurate and high-quality documents. You will frequently coordinate with clinical researchers, regulatory teams, and healthcare professionals to gather technical information, clarify data, and ensure compliance with industry standards. Communication is often managed through virtual meetings, email correspondence, and document review cycles, requiring strong interpersonal and project management skills. Building positive relationships with stakeholders helps streamline feedback and ensures the final deliverables meet both scientific and regulatory expectations.

What is the difference between Consultant Medical Writer vs Medical Writer?

AspectConsultant Medical WriterMedical Writer
CredentialsTypically requires a life sciences degree, advanced degree preferred, and relevant certificationsUsually holds a degree in life sciences, with or without additional certifications
Work EnvironmentOften works as a freelancer or contractor, collaborating with multiple clientsTypically employed by pharmaceutical or biotech companies, agencies, or CROs
Industry UsageCommonly used in consulting, freelance projects, and contract rolesWidely used within pharmaceutical, biotech, and healthcare industries

In summary, Consultant Medical Writers often work independently or as contractors, focusing on project-based work across various clients, while Medical Writers are usually employed full-time within organizations. Both roles require strong scientific knowledge and writing skills, but their work settings and employment types differ.

What are the key skills and qualifications needed to thrive as a consultant medical writer?

To thrive as a Consultant Medical Writer, you need a strong background in life sciences or medicine, excellent writing skills, and typically an advanced degree such as a PhD or PharmD. Familiarity with referencing software (e.g., EndNote), regulatory documentation systems, and guidelines like ICH or GPP3 is often required. Attention to detail, project management abilities, and clear communication help distinguish top performers in this field. These skills are vital for producing accurate, compliant, and impactful medical documents that support research, regulatory submissions, and scientific communication.

What is a consultant medical writer?

A Consultant Medical Writer is a professional who provides expert writing and editing services for medical and scientific documents, often on a freelance or contract basis. They typically work with pharmaceutical companies, research organizations, or healthcare communications agencies to develop materials such as clinical study reports, regulatory submissions, journal articles, and educational content. Their expertise combines scientific knowledge with strong communication skills to ensure complex medical information is accurately and clearly presented. Consultant Medical Writers may also advise clients on regulatory requirements and publication strategies. This role requires advanced degrees in life sciences or medicine and experience in medical writing.
More about Consultant Medical Writer jobs
Infographic showing various Consultant Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Medical Writer - Remote

YO AI Labs

Atlanta, GA โ€ข Remote

$50 - $90/hr

Full-time

Posted 3 days ago

New


Job description

Job Title: 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 evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing.

Key Responsibilities
  • Author and review Clinical Study Reports (CSRs) and other regulatory documents.

  • Interpret clinical protocols and ensure compliance with ICH guidelines.

  • Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.

  • Review safety documentation, including DSURs and PSURs/PBRERs.

  • Provide structured feedback and collaborate with cross-functional teams.

  • Support AI-assisted documentation evaluation and quality improvement initiatives.

Required Skills
  • Regulatory Medical Writing

  • Clinical Study Report (CSR) Authoring

  • ICH E3 Guidelines

  • Scientific Accuracy Assessment

  • Source Data Verification

  • Clinical Protocol Interpretation

  • TFL Analysis

  • eCTD Knowledge

  • Strong Written Communication & Collaboration

Qualifications
  • 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

  • Experience authoring Clinical Study Reports and regulatory documentation.

  • Strong knowledge of ICH E3, ICH E2F, ICH E2C, and eCTD requirements.

  • Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field (MD, PharmD, PhD, or MSc).

  • Experience in oncology and haematology is preferred.