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Ectd Data Analyst Jobs (NOW HIRING)

YO AI Labs

Medical Writer - Remote

Chicago, IL · Remote

$50 - $90/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

YO AI Labs

Clinical Document Author - Remote

Austin, TX · Remote

$50 - $80/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

YO AI Labs

Clinical Document Author - Remote

Chicago, IL · Remote

$50 - $80/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

YO AI Labs

Clinical Document Author - Remote

Atlanta, GA · Remote

$50 - $80/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

YO AI Labs

Medical Writer - Remote

Washington, DC · On-site

$50 - $80/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

YO AI Labs

Clinical Document Author - Remote

Phoenix, AZ · Remote

$50 - $80/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

YO AI Labs

Clinical Document Author - Remote

Houston, TX · Remote

$50 - $80/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

YO AI Labs

Clinical Document Author - Remote

Chicago, IL · On-site

$50 - $80/hr

Source Data Verification * Clinical Protocol Interpretation * TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing ...

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Ectd Data Analyst information

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How much do ectd data analyst jobs pay per year?

As of Sep 14, 2026, the average yearly pay for ectd data analyst in the United States is $82,640.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $97,000.00 per year, depending on experience, location, and employer.

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For Ectd Data Analyst jobs, the most frequently searched job titles are:

Infographic showing various Ectd Data Analyst job openings in the United States as of July 2026, with employment types broken down into 89% Full Time, 6% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 7% Hybrid, and 10% Remote job distribution, with an average salary of $82,640 per year, or $39.7 per hour.

Medical Writer - Remote

Chicago, IL • Remote

YO AI Labs
See more jobs at YO AI Labsexternal

$50 - $90/hr

Full-time

Re-posted 4 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.