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Author Consultant Jobs (NOW HIRING)

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

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

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

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

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

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Author Consultant information

What is the difference between Author Consultant vs Editor?

AspectAuthor ConsultantEditor
CredentialsWriting experience, industry knowledge, sometimes certifications in editing or publishingEditing certifications, strong language skills, experience in publishing
Work EnvironmentFreelance or consulting firms, client-based projectsPublishing houses, media companies, freelance editing
Employer & IndustryAuthors, publishing, media, marketingPublishing, media, corporate communications

While both Author Consultants and Editors work within the publishing and writing industry, Author Consultants primarily advise authors on content development, publishing strategies, and book marketing. Editors focus on reviewing, revising, and refining manuscripts to ensure clarity and quality. The roles often overlap but serve different stages of the publishing process, with Author Consultants guiding authors and Editors polishing the final product.

How to become an author consultant?

To become an author consultant, gain experience in writing, editing, or publishing, and develop strong communication and project management skills. Building a portfolio of successful projects and networking within the publishing industry can help establish credibility. Some consultants also pursue certifications in editing or publishing to enhance their expertise.

What cities are hiring for Author Consultant jobs?

Cities with the most Author Consultant job openings:

What states have the most Author Consultant jobs?

States with the most job openings for Author Consultant jobs include:

What are popular job titles related to Author Consultant jobs?

For Author Consultant jobs, the most frequently searched job titles are:

Clinical Document Author - Remote

Grapeland, TX โ€ข On-site

$50 - $80/hr

Other

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Job description

Job Description
Job Description
Job Title: Medical Writer / Clinical Document Author

Location: Remote
Job Type: Contractor
Pay: $50โ€“$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.