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Ai Regulation Jobs in Indiana (NOW HIRING)

micro1 AI

Medical Writing Manager

South Bend, IN · Remote

$50 - $80/hr

Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of ...

micro1 AI

Medical Billing Specialist

Fort Wayne, IN · Remote

$50 - $80/hr

Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of ...

micro1 AI

Medical Billing Specialist

Fishers, IN · Remote

$50 - $80/hr

Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of ...

micro1 AI

Director of Biostatistics

South Bend, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Director of Biostatistics

Fishers, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Biostatistician

Fishers, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Biostatistician

Fort Wayne, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Director of Biostatistics

Indianapolis, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Director of Biostatistics

Carmel, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Biostatistician

South Bend, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Director of Biostatistics

Fort Wayne, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Director of Biostatistics

Evansville, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Biostatistician

Carmel, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Biostatistician

Evansville, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

micro1 AI

Biostatistician

Indianapolis, IN · Remote

$60 - $100/hr

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific ...

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Showing results 41-60

All JobsAi Regulation JobsAi Regulation Jobs in Indiana

Ai Regulation information

What is the difference between Ai Regulation vs Data Privacy Officer?

AspectAi RegulationData Privacy Officer
Required CredentialsLegal or policy background, knowledge of AI systemsLegal, compliance, or privacy certifications (e.g., CIPP)
Work EnvironmentRegulatory agencies, tech companies, consulting firmsCorporate compliance departments, legal teams
Industry UsageAI development, tech regulation, policy makingData protection, privacy compliance, legal advisory

Ai Regulation professionals focus on creating and enforcing policies for AI systems, ensuring ethical and legal compliance. Data Privacy Officers primarily handle data protection policies, privacy laws, and safeguarding personal information. While both roles involve legal and compliance expertise, Ai Regulation emphasizes AI-specific policies, whereas Data Privacy Officers concentrate on data privacy laws and practices.

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Infographic showing various Ai Regulation job openings in Indiana as of August 2026, with employment types broken down into 76% Full Time, 21% Part Time, and 3% Contract. Highlights an 70% Physical, 3% Hybrid, and 27% Remote job distribution.

Medical Writer / Clinical Document Author

micro1 AI

Indianapolis, IN • Remote

$50 - $80/hr

Part-time

Posted 15 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