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YO AI Labs

Clinical Document Author - Remote

Houston, TX · Remote

$50 - $80/hr

Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong ...

YO AI Labs

Clinical Document Author - Remote

Addison, TX · On-site

$50 - $80/hr

Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong ...

VirTra

Be Seen First

Field Service Representative - AZ

Chandler, AZ · On-site

$25 - $28/hr

The Field Service Representative Tier 1 position is responsible for the initial configuration ... Conduct Video scenario authoring (IVR-100) training. * Conduct V-Marksmanship authoring training.

VirTra

Field Service Representative

Chandler, AZ · On-site

The Field Service Representative Tier 1 position is responsible for the initial configuration ... Conduct Video scenario authoring (IVR-100) training. * Conduct V-Marksmanship authoring training.

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As of Sep 10, 2026, the average hourly pay for author service representative in the United States is $23.03, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $27.40 per hour, depending on experience, location, and employer.

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Infographic showing various Author Service Representative job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $47,911 per year, or $23 per hour.

Clinical Document Author - Remote

Bellville, TX • On-site

YO AI Labs
See more jobs at YO AI Labsexternal

$50 - $80/hr

Other

This job post has expired 4 days ago. Applications are no longer accepted.

Job description

Job Description
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.

Apply