Pharmaceutical Subject Matter Expert – AI Model Evaluation

Posted 15 hours ago

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About the role

  • Pharmaceutical experts evaluating AI-generated regulatory, scientific, and manufacturing content for Volga Partners. Providing structured feedback to improve healthcare AI models.

Responsibilities

  • Evaluate AI-generated pharmaceutical content for scientific, technical, and regulatory accuracy, completeness, consistency, and compliance
  • Review information related to quality systems, manufacturing, validation, submissions, development, and compliance
  • Analyze whether AI-generated conclusions are supported by scientific principles, regulatory expectations, and industry best practices
  • Identify unsupported claims, technical inaccuracies, missing context, and flawed reasoning
  • Reference FDA requirements, GMP regulations, ICH guidelines, and accepted pharmaceutical industry practices
  • Provide expert feedback, explain findings, identify improvements, and recommend accurate corrections
  • Apply project-specific evaluation criteria, scoring guidelines, and quality standards
  • Complete independent evaluations using designated online platforms within project timelines

Requirements

  • Minimum of four years of relevant professional experience in the regulated US based pharmaceutical or biotechnology industry
  • Bachelor's degree or higher in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Engineering, Regulatory Affairs, or a related discipline
  • Strong expertise in at least one listed pharmaceutical specialty
  • Working knowledge of FDA requirements, GMP regulations, and relevant ICH guidelines, including applicable portions of ICH Q7-Q12
  • Ability to critically evaluate scientific, technical, and regulatory information
  • Strong analytical, research, and problem-solving abilities
  • Excellent written English communication skills
  • Confidence reviewing complex information and explaining technical conclusions
  • Comfort using digital platforms, web-based applications, and online research tools
  • Ability to work independently, follow detailed instructions, and meet established quality standards
  • Must understand and be comfortable with a task-based freelance engagement model
  • Preferred: PharmD, PhD, or advanced scientific credentials
  • Preferred: Experience preparing or reviewing regulatory submissions (IND, NDA, BLA, ANDA, MAA, or equivalent)
  • Preferred: Experience with FDA-regulated manufacturing, quality, compliance, validation, or development environments
  • Preferred: Experience performing quality reviews, regulatory audits, or scientific content evaluations
  • Preferred: Experience with technical writing, structured reviews, or compliance assessments
  • Preferred: Familiarity with AI model evaluation, prompt review, rubric development, or data annotation
  • Preferred: Previous involvement in scientific, regulatory, quality, or technical content assessment activities

Benefits

  • Remote work from an eligible location
  • Flexible, variable, assignment-based schedule
  • Project-based assignments with supplemental-income flexibility
  • Opportunity to contribute to advanced AI technologies
  • Experience contributing to AI evaluation initiatives
  • No AI background required

Job type

Contract

Experience level

Mid levelSenior

Salary

$20 - $50 per hour

Degree requirement

Bachelor's Degree

Location requirements

RemoteUnited States

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