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Remote International Medical Writer Jobs (NOW HIRING)

Veristat

  • Medical

  • Retirement

... International Council for Harmonisation (ICH) and other regulatory guidelines, and individual ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...

New

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Fully Remote (U.S.) Industry: Pharmaceutical / Biotechnology Employment Type: Full-Time Salary ... Medical Writer to support clinical development and regulatory documentation activities within a ...

Celerion

Medical Writer

OR · Remote

Good Clinical Practice, International Conference on Harmonisation guidelines) and client ... medical or clinical results. * Professional writing and editing skills for accurate and concise ...

Celerion

Medical Writer

Good Clinical Practice, International Conference on Harmonisation guidelines) and client ... medical or clinical results. * Professional writing and editing skills for accurate and concise ...

Celerion

Medical Writer

Good Clinical Practice, International Conference on Harmonisation guidelines) and client ... medical or clinical results. * Professional writing and editing skills for accurate and concise ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · Remote

Experience working in multicultural or remote team settings. * Proven ability to independently ... Strong understanding of International Council for Harmonization (ICH) guidelines and Good Clinical ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · Remote

Experience working in multicultural or remote team settings. * Proven ability to independently ... Strong understanding of International Council for Harmonization (ICH) guidelines and Good Clinical ...

Icon plc

Senior Medical Writer

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Medical Writer- ICON- Remote USA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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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How much do remote international medical writer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for remote international 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.
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Remote International Medical Writer jobs near you
Infographic showing various Remote International Medical Writer job openings in the United States as of August 2026, with employment types broken down into 71% Full Time, and 29% Part Time. Highlights an 100% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Medical Writer / Clinical Document - Remote

YO AI Labs

Miami, FL • Remote

$50 - $80/hr

Full-time

Posted 6 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.