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Remote Medical Writing Consultant Jobs (NOW HIRING)

Aston Carter

Remote Medical Coder

Memphis, TN · Remote

$75/hr

Remote Medical Coder Assess and validate AI-generated content related to healthcare operations ... Provide well-written, expert responses to operational healthcare scenarios for use in model ...

Travere

Manager, Medical Writing Operations

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... The Manager, Medical Writing Operations is responsible for leading document specialist support ...

Alnylam Pharmaceuticals

Senior Manager, Medical Writing

$146K - $197K/yr

... by consultants, contractors and vendors • Represent Medical Writing on multiple early phase ... Remote U.S. Pay Range $146,100.00 - $197,700.00 The pay range reflects the full-time base salary ...

Cardinal Health

... consulting services to pharmaceutical, biotechnology, and medical device companies worldwide. We ... Excellent interpersonal skills. #LI-Remote Candidates who are back-to-work, people with ...

Vaxcyte

Director, Clinical Medical Writing

San Carlos, CA · On-site +1

$221K - $258K/yr

Vaxcyte is seeking a Director, Clinical Medical Writing to drive and shape the medical writing ... San Carlos, CA or Remote Based Work Arrangement (may be adjusted based on business needs, job ...

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Remote Medical Writing Consultant information

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$31K

$148.2K

$399K

How much do remote medical writing consultant jobs pay per year?

As of Sep 3, 2026, the average yearly pay for remote medical writing consultant in the United States is $148,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $181,500.00 per year, depending on experience, location, and employer.

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

AspectRemote Medical Writing ConsultantRemote Medical Writer
CredentialsTypically requires advanced degrees (e.g., MD, PhD, PharmD) and industry certificationsOften requires a degree in life sciences or related field; certifications are a plus
Work EnvironmentConsults with clients, provides strategic guidance, and reviews documentsPrepares, writes, and edits scientific and regulatory documents
Employer & Industry UsageConsulting firms, pharmaceutical companies, CROsPharmaceutical, biotech, and healthcare companies

Remote Medical Writing Consultants focus on providing expert advice, strategic input, and review services, often working on complex projects. Remote Medical Writers primarily produce and edit scientific and regulatory documents. Both roles require strong scientific knowledge, but the consultant role emphasizes strategic oversight and client interaction, while the writer role centers on document creation and editing.

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The most popular types of Medical Writing Consultant jobs are:

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Remote Medical Writing Consultant jobs near you
Infographic showing various Remote Medical Writing Consultant 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 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $148,159 per year, or $71.2 per hour.

Medical Writer / Clinical Document - Remote

YO AI Labs

Statesville, NC • Remote

$50 - $80/hr

Full-time

Posted 23 days ago

Job description

Job Title: Medical Writer / Clinical Document Author

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.