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Remote Associate Medical Writer Jobs in California

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 ...

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 ...

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 ...

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 ...

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 ...

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology ...

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology ...

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Remote Associate Medical Writer information

What is the difference between Remote Associate Medical Writer vs Medical Writer?

AspectRemote Associate Medical WriterMedical Writer
CredentialsBachelor's degree in life sciences; often a master's or PhD preferredBachelor's or higher in life sciences; advanced degrees common
Work EnvironmentRemote, collaborative teams, often entry-levelRemote or onsite, more experienced roles
Industry UsageEntry-level or early-career medical writing roles in pharma/biotechMid to senior-level medical writing across various projects
Search & Comparison IntentOften searched by those starting in medical writing or seeking entry-level rolesCompared for experienced roles or career advancement

The Remote Associate Medical Writer typically is an entry-level position requiring relevant life sciences credentials and is often remote. Medical Writers may have more experience and handle complex projects. Both roles are common in pharma and biotech industries, but the Associate role is ideal for those beginning their medical writing careers.

What are the most commonly searched types of Remote Medical Writer jobs in California?

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

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

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

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

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

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

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

Infographic showing various Remote Associate 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

Palo Alto, CA • Remote

$50 - $90/hr

Full-time

Posted 15 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.