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Remote Regulatory Medical Writer Jobs in Romeoville, IL

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Author and review Clinical Study Reports (CSRs) and other regulatory documents. * Interpret ...

Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical ... Required Skills * Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 ...

Medical Writing Manager

Joliet, IL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Medical Writing Manager

Aurora, IL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

... writing and medical device regulatory affairs or a Ph.D. with at least 3 years of experience Location & Travel Requirements * This is a remote role (candidates must be based in the United States)

Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Experience with complex medical devices, such as some combination of: * Genomics * NGS * Software ...

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Remote Regulatory Medical Writer information

See Romeoville, IL salary details

$14

$39

$59

How much do remote regulatory medical writer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for remote regulatory medical writer in Romeoville, IL is $39.39, according to ZipRecruiter salary data. Most workers in this role earn between $26.73 and $49.76 per hour, depending on experience, location, and employer.

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

AspectRemote Regulatory Medical WriterRemote Medical Writer
CredentialsMedical degree, regulatory writing experience, certifications (e.g., RAC)Medical, scientific, or related degree; writing experience
Work EnvironmentPharmaceutical/biotech companies, CROs, regulatory agenciesPharmaceutical, biotech, healthcare, or scientific organizations
Industry UsageRegulatory submissions, INDs, NDAs, safety reportsResearch publications, clinical trial documentation, scientific publications
Search/Comparison IntentRegulatory documentation, compliance, submission writingScientific writing, research, publication

The main difference is that Remote Regulatory Medical Writers focus on preparing regulatory documents for drug approvals and compliance, often requiring specific regulatory knowledge and certifications. Remote Medical Writers have a broader scope, including scientific publications and research documentation. Both roles require strong writing skills and relevant scientific backgrounds, but Regulatory Medical Writers specialize in regulatory submissions and compliance processes.

What are the most commonly searched types of Regulatory Medical Writer jobs in Romeoville, IL?

The most popular types of Regulatory Medical Writer jobs in Romeoville, IL are:

What are popular job titles related to Remote Regulatory Medical Writer jobs in Romeoville, IL?

For Remote Regulatory Medical Writer jobs in Romeoville, IL, the most frequently searched job titles are:

What job categories do people searching Remote Regulatory Medical Writer jobs in Romeoville, IL look for?

The top searched job categories for Remote Regulatory Medical Writer jobs in Romeoville, IL are:

What cities near Romeoville, IL are hiring for Remote Regulatory Medical Writer jobs?

Cities near Romeoville, IL with the most Remote Regulatory Medical Writer job openings:

Medical Writer - Remote

YO AI Labs

Chicago, IL • Remote

$50 - $90/hr

Full-time

Posted 10 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.