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Director Remote Medical Writing Jobs in Washington

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Job Title: Medical Coder Job Type: Contractor Location: Remote Job Overview We are seeking ... Collaborate with project teams through written and verbal communication to improve AI training data ...

Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ... Excellent written communication skills with the ability to explain complex clinical concepts ...

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Director Remote Medical Writing information

What is the difference between Director Remote Medical Writing vs Medical Writing Manager?

AspectDirector Remote Medical WritingMedical Writing Manager
CredentialsTypically requires advanced degrees (MD, PhD, PharmD) and extensive medical writing experienceRequires similar credentials but may have slightly less experience or seniority
Work EnvironmentLeads remote medical writing teams, collaborates with cross-functional teams, and oversees project strategyManages medical writing staff, reviews documents, and ensures quality and compliance
Industry UsageCommonly used in pharmaceutical, biotech, and healthcare industries for strategic oversightUsed across similar industries for team management and project execution

The main difference is that the Director Remote Medical Writing typically holds a higher strategic leadership role with broader responsibilities, while the Medical Writing Manager focuses more on team management and document quality. Both roles require strong medical writing credentials and industry experience, but the director position involves more oversight and strategic planning.

What are popular job titles related to Director Remote Medical Writing jobs in Washington?

For Director Remote Medical Writing jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Director Remote Medical Writing jobs in Washington look for?

The top searched job categories for Director Remote Medical Writing jobs in Washington are:

What cities in Washington are hiring for Director Remote Medical Writing jobs?

Cities in Washington with the most Director Remote Medical Writing job openings:

Infographic showing various Director Remote Medical Writing job openings in Washington as of June 2026, with employment types broken down into 64% Full Time, 19% Part Time, and 17% Contract. Highlights an 100% Remote job distribution.

Medical Writer - Remote

YO AI Labs

Washington, DC • Remote

$50 - $90/hr

Full-time

Posted 9 days ago


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.