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Overnight Medical Writing Consultant Jobs (NOW HIRING)

... 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 ...

Medical Writer

Boston, MA · On-site

$55 - $70/hr

Medical Writing Science Manager 📍 Boston, MA | Hybrid -- 3 days onsite / 2 days remote 💼 Initial 2-month contract | Potential for extension or conversion 💰 $55-$70/hour ⏰ 40 hours/week We ...

... consulting services to pharmaceutical, biotechnology, and medical device companies worldwide. We ... Write, review, and/or edit clinical regulatory documents such as CTD Module 2 summaries and ...

... 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 ...

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

... 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 ...

Medical Writer - Remote

Miami, FL · Remote

$50 - $90/hr

... 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 ...

... 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 ...

... 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 ...

Medical Writer - Remote

Dallas, TX · Remote

$50 - $90/hr

... 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 ...

... 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 ...

... 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 ...

... 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 ...

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

... 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 ...

... 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 ...

... 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 ...

Medical Writer - Remote

San Jose, CA · On-site

$69 - $110/hr

... 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 ...

Overnight Medical Scribe

Forney, TX · On-site

$10 - $12/hr

... consultations. - Record diagnosis, discharge, prescriptions, and/or follow-up instructions ... medical terminology is preferred - Ability to type a minimum of 50 WPM - Punctual - Flexible ...

Showing results 21-40

Overnight Medical Writing Consultant information

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$31K

$148.2K

$399K

How much do overnight medical writing consultant jobs pay per year?

As of Sep 3, 2026, the average yearly pay for overnight medical writing consultant in the United States is $148,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $181,500.00 per year, depending on experience, location, and employer.

What cities are hiring for Overnight Medical Writing Consultant jobs?

Cities with the most Overnight Medical Writing Consultant job openings:

What are the most commonly searched types of Medical Writing Consultant jobs?

The most popular types of Medical Writing Consultant jobs are:

What states have the most Overnight Medical Writing Consultant jobs?

States with the most job openings for Overnight Medical Writing Consultant jobs include:

Infographic showing various Overnight Medical Writing Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $148,159 per year, or $71.2 per hour.

Medical Writer - Remote

YO AI Labs

Philadelphia, PA • Remote

$50 - $90/hr

Full-time

Posted 22 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.