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Medical Writing Jobs Near Me

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 ...

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates ...

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 ...

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... medical device or biotechnology companies. Or High School Diploma / GED and 8 years in ... writing. Experience with device assembly and packaging of final product. Ability to translate ...

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Technical Writer

Delaware, OH · On-site +1

$55K - $65K/yr

AI-Assisted Writing: Leverage integrated AI tools (such as Gemini) to optimize initial engineering ... Incentive Bonus Plans * Medical, Dental, Visionbenefits * 401K with Company Match * 10 Paid ...

Exceptional persuasive writing skills with the ability to tell a clear and compelling story ... with company match, medical, dental, vision, life insurance, AD&D, flexible spending account ...

Grant Writer

Columbus, OH · On-site

$64K - $91K/yr

... writing, management, and reporting of grants. The position may participate in or assist in leading ... Facilities are a medical office environment with front-desk reception area, separate patient ...

Medical Technologist

Columbus, OH · On-site

$35.71 - $51.78/hr

Write and update department rule books Medical Technologist Qualifications: * A bachelor's degree in Clinical Laboratory Science or a related field is required * ASCP or AMT Certification is Required ...

Medical Technologist

Columbus, OH · On-site

$35.71 - $51.78/hr

Write and update department rule books Medical Technologist Qualifications: * A bachelor's degree in Clinical Laboratory Science or a related field is required * ASCP or AMT Certification is Required ...

Medical Technologist

Columbus, OH · On-site

$35.71 - $51.78/hr

Write and update department rule books Medical Technologist Qualifications: * A bachelor's degree in Clinical Laboratory Science or a related field is required * ASCP or AMT Certification is Required ...

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Medical Writing information

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How much do medical writing jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for medical writing in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.
What cities are hiring for Medical Writing jobs? Cities with the most Medical Writing job openings:
What states have the most Medical Writing jobs? States with the most job openings for Medical Writing jobs include:
What are the most commonly searched types of Medical Writing jobs? The most popular types of Medical Writing jobs are:
A map of the United States highlighting the number of Medical Writing job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Medical Writing job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Medical Writing Manager

micro1 AI

Columbus, OH • Remote

$50 - $80/hr

Part-time

Posted 4 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.