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Documentation Writer Jobs Near Me

Edit documents for spelling, grammar, clarity, consistency, content accuracy, readability, and ... writing standards, and formatting conventions. * Coordinate with cross functional teams during ...

Technical Writer

Delaware, OH · On-site +1

$55K - $65K/yr

Global Customer Documentation is seeking a detail-oriented, highly collaborative Technical Writer to join our team in planning, designing, and maintaining high-quality technical documentation. In ...

Edit documents for spelling, grammar, clarity, consistency, content accuracy, readability, and ... writing standards, and formatting conventions. * Coordinate with cross functional teams during ...

Technical Writer (TW3) is needed for the Modernization / Re-write of a .NET Application. The TW3 ... Document current state and future state workflows, including Intake Process, Billing Flows ...

Grant Writer

Columbus, OH · On-site

$64K - $91K/yr

Identify and write grants to secure funding for projects in the organization ... Gathers letters of support and other documents needed for grant applications. * Coordinate with ...

Write, edit, and produce persuasive content for proposals, corporate databases, sales documents, and other business development-related projects. * Information Sourcing : Identify and gather relevant ...

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

As a Lead Medical Writer on a 2-month remote contract, you will autonomously author and review a range of clinical regulatory documents, including CTD Module II summaries, Clinical Overviews ...

Working with Finance and IT to create various documentation for existing systems. Create User ... Strong communication skills: both written and spoken. Work with Application Team members to enhance ...

The TW3 would be responsible for all Technical Documentation, Business Process descriptions, system ... Technical Writer activities. · Develop and manage short and long-term documentation plans and ...

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Effective written and verbal communication skills. * Ability to work onsite in Columbus five days ... Commercial credit and loan documentation * Advanced Excel: VLOOKUP, XLOOKUP, and PivotTables

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How much do documentation writer jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for documentation writer in the United States is $35.98, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $50.00 per hour, depending on experience, location, and employer.
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What states have the most Documentation Writer jobs? States with the most job openings for Documentation Writer jobs include:
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A map of the United States highlighting the number of Documentation Writer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Documentation Writer job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Medical Writer / Clinical Document Author

micro1 AI

Columbus, OH • Remote

$50 - $80/hr

Part-time

Posted 5 days ago


Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.