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Director Remote Medical Writing Jobs in Boston, MA

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

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

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

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

A minimum of 3 years medical writing experience. Direct experience working on clinical evaluations ... LI-remote About us With a firm belief that every person and community should have access to the ...

A minimum of 3 years medical writing experience. Direct experience working on clinical evaluations ... LI-remote About us With a firm belief that every person and community should have access to the ...

Senior Principal Medical Writer

Billerica, MA · On-site +1

$126K - $215K/yr

Acting as the primary medical writing lead within cross-functional teams, you will define document ... Vendor management and remote leadership * Strong communication, negotiation, and stakeholder ...

Senior Principal Medical Writer

Billerica, MA · On-site +1

$126K - $215K/yr

Acting as the primary medical writing lead within cross-functional teams, you will define document ... Vendor management and remote leadership * Strong communication, negotiation, and stakeholder ...

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Director Remote Medical Writing information

See Boston, MA salary details

$14.1K

$252.4K

$387.8K

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

As of Aug 30, 2026, the average yearly pay for director remote medical writing in Boston, MA is $252,445.00, according to ZipRecruiter salary data. Most workers in this role earn between $215,100.00 and $309,100.00 per year, depending on experience, location, and employer.

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 the most commonly searched types of Remote Medical Writing jobs in Boston, MA?

The most popular types of Remote Medical Writing jobs in Boston, MA are:

What are popular job titles related to Director Remote Medical Writing jobs in Boston, MA?

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

What job categories do people searching Director Remote Medical Writing jobs in Boston, MA look for?

The top searched job categories for Director Remote Medical Writing jobs in Boston, MA are:

Medical Writer - Remote

Boston, MA • Remote

$50 - $90/hr

Full-time

Posted 19 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.