ZipRecruiter

Log In

1

Remote Scientific Writer Jobs Near Me

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 ...

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 ...

VIVA USA INC

Technical Writer

Columbus, OH · On-site

Technical Writer (TW3) is needed for the Modernization / Re-write of a .NET Application. The TW3 ... Education: 4 year college Degree in IT, Computer Science, Engineering or Business with a focus on ...

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 ...

KBR

Proposal Writer

Columbus, OH · On-site

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 ...

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 ...

next page

Showing results 1-20

All JobsRemote Scientific Writer JobsRemote Scientific Writer Jobs Near Me

Remote Scientific Writer information

See salary details

$21

$47

$73

How much do remote scientific writer jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for remote scientific writer in the United States is $47.12, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $58.65 per hour, depending on experience, location, and employer.
More about Remote Scientific Writer jobs
What are popular job titles related to Remote Scientific Writer jobs? For Remote Scientific Writer jobs, the most frequently searched job titles are:
What job categories do people searching Remote Scientific Writer jobs look for? The top searched job categories for Remote Scientific Writer jobs are:
What cities are hiring for Remote Scientific Writer jobs? Cities with the most Remote Scientific Writer job openings:
What states have the most Remote Scientific Writer jobs? States with the most job openings for Remote Scientific Writer jobs include:
What are the most commonly searched types of Scientific Writer jobs? The most popular types of Scientific Writer jobs are:
Remote Scientific Writer jobs near you
A map of the United States highlighting the number of Remote Scientific Writer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Remote Scientific Writer job openings in each state, with California having the most at 2 and Alaska the least at 0.

Medical Writer / Clinical Document Author

micro1 AI

Columbus, OH • Remote

$50 - $80/hr

Part-time

This job post has expired today. Applications are no longer accepted.

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