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Assistant Remote Medical Writing Jobs in New York

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

Medical Writing Job Category: Professional All Job Posting Locations: Horsham, Pennsylvania, United ... The position is Hybrid (3 days onsite weekly). (Remote work options may be considered on a case-by ...

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Assistant Remote Medical Writing information

Is there a demand for assistant remote medical writers?

There is a growing demand for assistant remote medical writers due to the increasing need for clear scientific communication in healthcare, pharmaceuticals, and biotech industries. These roles often require strong writing skills, familiarity with medical terminology, and the ability to work independently in a remote environment, with opportunities expanding as remote work becomes more accepted in the field.

What are the most commonly searched types of Remote Medical Writing jobs in New York?

The most popular types of Remote Medical Writing jobs in New York are:

What are popular job titles related to Assistant Remote Medical Writing jobs in New York?

For Assistant Remote Medical Writing jobs in New York, the most frequently searched job titles are:

What cities in New York are hiring for Assistant Remote Medical Writing jobs?

Cities in New York with the most Assistant Remote Medical Writing job openings:

Infographic showing various Assistant Remote Medical Writing job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution.

Medical Writer - Remote

YO AI Labs

New York, NY • Remote

$50 - $80/hr

Full-time

Posted 20 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.