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Remote Pfizer Medical Writer Jobs in California (NOW HIRING)

YO AI Labs

Medical Writer - Remote

Palo Alto, CA · Remote

$50 - $90/hr

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 ...

YO AI Labs

Medical Writer - Remote

Los Angeles, CA · Remote

$50 - $90/hr

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 ...

YO AI Labs

Medical Writer - Remote

San Francisco, CA · Remote

$50 - $90/hr

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 ...

YO AI Labs

Medical Writer - Remote

San Jose, CA · Remote

$50 - $90/hr

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 ...

Veristat

Principal Medical Writer

Ontario, CA · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ...

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All JobsPfizer Medical Writer JobsRemote Pfizer Medical Writer JobsRemote Pfizer Medical Writer Jobs in California

Remote Pfizer Medical Writer information

What is the difference between Remote Pfizer Medical Writer vs Remote Medical Science Liaison?

AspectRemote Pfizer Medical WriterRemote Medical Science Liaison
Required CredentialsMedical degree or life sciences background, writing certificationsMedical or scientific degree, often with clinical or research experience
Work EnvironmentCollaborates with medical teams, writes regulatory and scientific documentsEngages with healthcare professionals, provides scientific education
Employer & Industry UsagePharmaceutical companies, biotech firms, regulatory agenciesPharmaceutical companies, medical organizations, biotech firms

Remote Pfizer Medical Writers focus on creating scientific and regulatory documents within pharmaceutical companies, while Remote Medical Science Liaisons primarily engage with healthcare professionals to communicate scientific information. Both roles require strong scientific credentials but differ in daily tasks and interactions.

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The most popular types of Pfizer Medical Writer jobs in California are:

What are popular job titles related to Remote Pfizer Medical Writer jobs in California?

For Remote Pfizer Medical Writer jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Pfizer Medical Writer jobs in California look for?

The top searched job categories for Remote Pfizer Medical Writer jobs in California are:

What cities in California are hiring for Remote Pfizer Medical Writer jobs?

Cities in California with the most Remote Pfizer Medical Writer job openings:

Remote Pfizer Medical Writer jobs near you
Infographic showing various Remote Pfizer Medical Writer job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Medical Writer - Remote

YO AI Labs

Palo Alto, CA • Remote

$50 - $90/hr

Full-time

Posted 6 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.