1

Director Ai Writer Jobs in Indiana (NOW HIRING)

... AI. Preferred Qualifications * Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the ...

... AI. Preferred Qualifications * Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the ...

... AI. Preferred Qualifications * Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the ...

Medical Writing Manager

Carmel, IN · Remote

$50 - $80/hr

... AI. Preferred Qualifications * Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the ...

... AI. Preferred Qualifications * Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the ...

... AI. Preferred Qualifications * Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience independently authoring or leading the ...

About Markup AI Markup AI is pioneering the AI content governance category with the industry ... Excellent written and verbal communicator, comfortable presenting strategy and results to executive ...

About Markup AI Markup AI is pioneering the AI content governance category with the industry ... Excellent written and verbal communicator, comfortable presenting strategy and results to executive ...

next page

Showing results 1-20

Director Ai Writer information

What is the difference between Director Ai Writer vs Content Strategist?

AspectDirector Ai WriterContent Strategist
Required CredentialsBachelor's degree in Communications, Marketing, or related field; experience with AI toolsBachelor's degree in Marketing, Communications, or related field; experience in content planning
Work EnvironmentCollaborates with AI teams, marketing, and content creators in corporate or agency settingsWorks on content planning, audience analysis, and campaign development across various industries
Employer & Industry UsageUsed in tech, marketing agencies, and media companies focusing on AI-driven contentCommon in marketing departments, media firms, and digital agencies

The main difference is that a Director Ai Writer oversees AI-driven content creation processes, focusing on managing AI tools and teams, while a Content Strategist develops overall content plans and strategies to engage target audiences. Both roles require strong communication skills and industry knowledge but differ in their focus on AI technology versus content planning.

What are the most commonly searched types of Ai Writer jobs in Indiana?

The most popular types of Ai Writer jobs in Indiana are:

What are popular job titles related to Director Ai Writer jobs in Indiana?

For Director Ai Writer jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Director Ai Writer jobs in Indiana look for?

The top searched job categories for Director Ai Writer jobs in Indiana are:

What cities in Indiana are hiring for Director Ai Writer jobs?

Cities in Indiana with the most Director Ai Writer job openings:

Infographic showing various Director Ai Writer job openings in Indiana as of June 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, 1% Temporary, and 4% Contract. Highlights an 66% Physical, 3% Hybrid, and 31% Remote job distribution.

Medical Writer / Clinical Document Author

micro1 AI

South Bend, IN • Remote

$50 - $80/hr

Part-time

Posted 12 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.