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Director Ai Writer Jobs in Indiana (NOW HIRING)

No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work ... Provide structured written rationales distinguishing true statistical errors from acceptable ...

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

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

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

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

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

Showing results 21-40

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 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.

Director of Biostatistics

micro1 AI

Evansville, IN • Remote

$60 - $65/hr

Part-time

Re-posted 2 days ago


Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. 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 evaluation tasks that require deriving, reproducing, or validating statistical outputs from clinical datasets and associated tables, figures, and listings (TFLs).
  2. Apply expert judgment to assess the correctness and consistency of reported estimates, confidence intervals, p-values, analysis populations, and missing data handling in alignment with the statistical analysis plan (SAP).
  3. Identify discrepancies between statistical outputs and their narrative descriptions in clinical study reports (CSR), including subtle errors in population definitions, censoring rules, or multiplicity handling.
  4. Establish defensible ground truth for each evaluation task, documenting the derivation process to enable independent verification.
  5. Provide structured written rationales distinguishing true statistical errors from acceptable methodological alternatives, employing clear and concise communication.
  6. Collaborate with a multidisciplinary project team, providing statistical insights and feedback as needed to refine evaluation tasks and criteria.


Preferred Qualifications

  1. 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit.
  2. Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets.
  3. Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies under ICH E9(R1).
  4. Proficiency in SAS and/or R, with the ability to independently reproduce analyses from written specifications.
  5. Ability to interpret SAPs and ensure reported results are consistent with pre-specified analyses.
  6. Advanced degree (MSc or PhD) in Biostatistics, Statistics, or a closely related quantitative field.
  7. Nice to have: Experience as lead statistician on pivotal/registrational studies, authoring or reviewing CSR statistical sections, oncology endpoint expertise, and exposure to AI-assisted statistical review tools.