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Remote Clinical Protocol Writer Jobs in Chicago, IL

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Interpret clinical protocols and ensure compliance with ICH guidelines. * Verify scientific ...

Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical ... Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication ...

Medical Writing Manager

Elgin, IL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Medical Writing Manager

Aurora, IL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Medical Writing Manager

Joliet, IL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Protocol Coordinator

Chicago, IL · On-site +1

$60K - $85K/yr

The Alliance develops and conducts clinical trials with promising new cancer therapies and utilizes ... Strong oral and written skills. * Decision-making skills. * Strong interpersonal and customer ...

Clinicia Expert - Remote

Chicago, IL · Remote

$150 - $200/hr

Provide structured, guideline-based written explanations of clinical reasoning and findings ... Experience reviewing clinical trial documents, including protocols, investigator brochures ...

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Remote Clinical Protocol Writer information

See Chicago, IL salary details

$25

$55

$85

How much do remote clinical protocol writer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for remote clinical protocol writer in Chicago, IL is $55.99, according to ZipRecruiter salary data. Most workers in this role earn between $41.11 and $66.11 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Clinical Protocol Writer jobs in Chicago, IL?

The most popular types of Clinical Protocol Writer jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Remote Clinical Protocol Writer jobs?

Cities near Chicago, IL with the most Remote Clinical Protocol Writer job openings:

Infographic showing various Remote Clinical Protocol Writer job openings in Chicago, IL as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $116,455 per year, or $56 per hour.

Medical Writer / Clinical Document - Remote

YO AI Labs

Chicago, IL • Remote

$50 - $80/hr

Full-time

Posted 12 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.