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Pharmaceutical Subject Matter Expert – AI Model Evaluation
Volga Partners. Evaluate AI-generated pharmaceutical content for accuracy, completeness, consistency, and compliance with industry standards .
Posted 10/27/2026contractRemote • United States, Philippines, Indonesia, Singapore, VietnamMid-LevelSenior💰 $20 - $50 per hourWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in evaluating AI-generated pharmaceutical content for accuracy and compliance with FDA requirements, GMP regulations, and ICH guidelines. Possesses strong analytical and problem-solving skills, with the ability to communicate complex technical information effectively.
Highest-signal resume keywords
Pharmaceutical Industry ExpertiseFDA Requirements KnowledgeGMP Regulations FamiliarityAnalytical SkillsTechnical Writing Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Pharmaceutical Content EvaluationRegulatory Submissions PreparationQuality ReviewScientific AnalysisCompliance Assessment
Soft Skills
Excellent Written CommunicationProblem-Solving AbilitiesIndependent Work Capability
Tools & Technologies
Digital PlatformsWeb-Based ApplicationsOnline Research Tools
Certifications & Qualifications
PharmDPhD
Industry Keywords
AI Model EvaluationICH GuidelinesQuality SystemsValidationRegulatory Affairs
About the role
Key responsibilities & impact- Evaluate AI-generated pharmaceutical content for accuracy, completeness, consistency, and compliance with industry standards
- Review scientific and regulatory 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 to validate information
- Provide expert feedback, explain findings, and recommend technically accurate corrections
- Apply project-specific evaluation criteria, scoring guidelines, and quality standards to support AI quality improvement
- Complete independent evaluations using designated online platforms within established project timelines
Requirements
What you’ll need- 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
Benefits
Comp & perks- Remote work
- Flexible, variable, assignment-based schedule
- Project-based freelance work
- Opportunity to contribute to advanced AI technologies
- Supplemental-income opportunity
- No AI background required