ZipRecruiter

Log In

1

Contract Medical Writer Clinical Research Jobs (NOW HIRING)

Solventum

Medical Writer - Clinical Compliance

$124K - $170K/yr

Medical Writer - Clinical Compliance(Solventum) 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of ...

YO AI Labs

Medical Writer - Remote

Atlanta, GA · Remote

$50 - $90/hr

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 ...

next page

Showing results 1-20

All Jobsfreelance JobsEducation JobsBusiness Education JobsScientific Writer JobsContract Medical Writer Clinical Research Jobs

Contract Medical Writer Clinical Research information

See salary details

$11

$46

$78

How much do contract medical writer clinical research jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for contract medical writer clinical research in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

What cities are hiring for Contract Medical Writer Clinical Research jobs?

Cities with the most Contract Medical Writer Clinical Research job openings:

What are the most commonly searched types of Medical Writer Clinical Research jobs?

The most popular types of Medical Writer Clinical Research jobs are:

What states have the most Contract Medical Writer Clinical Research jobs?

States with the most job openings for Contract Medical Writer Clinical Research jobs include:

Contract Medical Writer Clinical Research jobs near you

Medical Writer / Clinical Document - Remote

San Jose, CA • Remote

YO AI Labs
See more jobs at YO AI Labsexternal

$50 - $80/hr

Full-time

Posted 21 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.