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Full Time Medical Writer Clinical Research Jobs (NOW HIRING)

Solventum

Medical Writer - Clinical Compliance

$124K - $170K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

New York, NY · Remote

$50 - $80/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 ...

YO AI Labs

Medical Writer - Remote

Palo Alto, CA · 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 ...

YO AI Labs

Medical Writer - Remote

Austin, TX · 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 ...

YO AI Labs

Medical Writer - Remote

Seattle, WA · 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 ...

YO AI Labs

Medical Writer - Remote

Chicago, IL · 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 ...

YO AI Labs

Medical Writer - Remote

Phoenix, AZ · 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 ...

YO AI Labs

Medical Writer - Remote

Washington, DC · 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 ...

YO AI Labs

Medical Writer - Remote

Seattle, WA · 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 ...

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Full Time Medical Writer Clinical Research information

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

As of Aug 20, 2026, the average hourly pay for full time 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 is the difference between Full Time Medical Writer Clinical Research vs Medical Writer Clinical Research?

AspectFull Time Medical Writer Clinical ResearchMedical Writer Clinical Research
CredentialsTypically requires a degree in life sciences or related field; certifications like AMWA or EMWA are commonSame as above; often holds similar qualifications and certifications
Work EnvironmentFull-time employment in pharmaceutical, biotech, or CRO settings; office or remote workSimilar environment; may include freelance or contract roles in the same industries
Employer & Industry UsageEmployed by pharmaceutical companies, CROs, or biotech firms; focused on regulatory and scientific documentationUsed interchangeably; both roles involve scientific writing for clinical trials and regulatory submissions

In summary, Full Time Medical Writer Clinical Research and Medical Writer Clinical Research share similar qualifications, work environments, and industry usage. The main difference is that the full-time role involves permanent employment, whereas the other may include freelance or contract positions. Both roles focus on creating scientific and regulatory documents for clinical research.

What cities are hiring for Full Time Medical Writer Clinical Research jobs?

Cities with the most Full Time 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 Full Time Medical Writer Clinical Research jobs?

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

Full Time Medical Writer Clinical Research jobs near you

Medical Writer / Clinical Document - Remote

YO AI Labs

San Jose, CA • Remote

$50 - $80/hr

Full-time

Posted 9 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.