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Scientific Writer Jobs Near Me

KBR

Proposal Writer

Columbus, OH

KBR's areas of expertise include engineering, logistics, operations, science, program management ... As a Proposal Writer at KBR, you will play a pivotal role in crafting compelling narratives that ...

micro1 AI

Medical Writing Manager

Columbus, OH · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Comtech Global

Technical Writer 3

Columbus, OH · On-site

A Technical Writer (TW3) is needed for the Modernization / Re-write of a .NET Application. The TW3 ... Educational requirements: · Education: 4 year college Degree in IT, Computer Science, Engineering ...

Manifest Solutions

Technical Writer

Columbus, OH · On-site

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

Manifest Solutions

Technical Writer

Columbus, OH

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

Wellington Management

RFP Writer

London, OH · On-site

Overview The Global RFP Team is seeking an RFP Writer to support the completion of prospect proposals, client questionnaires, and other strategic client deliverables. The team is responsible for ...

Wellington Management

RFP Writer

London, OH

Overview The Global RFP Team is seeking an RFP Writer to support the completion of prospect proposals, client questionnaires, and other strategic client deliverables. The team is responsible for ...

Merck & Co.

Specialist Technical Writing

New Albany, OH · On-site

$70 - $100/hr

Master's Degree in Science and/or Engineering. * Or * Bachelor's Degree in Science and/or ... writing. * Experience with device assembly and packaging of final product. * Ability to translate ...

New

IDEALFORCE LLC

Technical Writer (39831)

Columbus, OH · On-site

Strong communication skills: both written and spoken. Work with Application Team members to enhance their understanding of end-user and technical documentation. Ensure messages and terminology is ...

Wing Assistant

Content Writer (US)

Columbus, OH · Remote

$3.7K/wk

Content Writer (Remote) Wing is on the exciting mission of redefining the future of work for companies worldwide! We are looking to be the one-stop shop for companies that are looking to build world ...

Wing Assistant

Content Writer (US)

Columbus, OH · On-site +1

Content Writer (Remote) Wing is on the exciting mission of redefining the future of work for companies worldwide! We are looking to be the one-stop shop for companies that are looking to build world ...

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As of Aug 20, 2026, the average yearly pay for scientific writer in the United States is $70,499.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,000.00 and $74,000.00 per year, depending on experience, location, and employer.
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Scientific Writer jobs near you
A map of the United States highlighting the number of Scientific Writer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Scientific 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 17 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.

Apply