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Full Time Regulatory Medical Writer Jobs (NOW HIRING)

Telix Pharmaceuticals (AMER)

Medical Writer

OR · On-site +1

This role will provide medical writing support by organizing, analyzing, and interpreting ... Such documents include all types of regulatory documents, including eCTD summary documents (for ...

Syneos Health

Sr. Medical Writer (Regulatory)

Sr. Medical Writer (Regulatory) Syneos Health ® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point ...

Telix Pharmaceuticals

Medical Writer

This role will provide medical writing support by organizing, analyzing, and interpreting ... Such documents include all types of regulatory documents, including eCTD summary documents (for ...

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All JobsRegulatory Medical Writer JobsFull Time Regulatory Medical Writer Jobs

Full Time Regulatory Medical Writer information

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$57

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

As of Aug 14, 2026, the average hourly pay for full time regulatory medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is the difference between Full Time Regulatory Medical Writer vs Clinical Writer?

AspectFull Time Regulatory Medical WriterClinical Writer
Required CredentialsLife sciences degree, medical or scientific background, often regulatory certificationsLife sciences degree, scientific background, may have regulatory or clinical certifications
Work EnvironmentPharmaceutical, biotech, or regulatory agencies; office or remoteClinical research organizations, pharmaceutical companies, or academic settings
Employer & Industry UsagePrimarily in regulatory affairs within pharma/biotechIn clinical research, data analysis, and study documentation

Full Time Regulatory Medical Writers focus on preparing regulatory documents for drug approval processes, requiring regulatory knowledge and certifications. Clinical Writers typically work on clinical study reports and protocols, often with a clinical research background. While both roles require scientific expertise, Regulatory Medical Writers specialize in regulatory submissions, whereas Clinical Writers focus on clinical trial documentation.

What cities are hiring for Full Time Regulatory Medical Writer jobs?

Cities with the most Full Time Regulatory Medical Writer job openings:

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

The most popular types of Regulatory Medical Writer jobs are:

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Full Time Regulatory Medical Writer jobs near you

Medical Writer / Clinical Document - Remote

YO AI Labs

Boston, MA • Remote

$50 - $80/hr

Full-time

Posted 4 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.