Pharmaceutical Subject Matter Expert (SME) - AI Model Evaluation (US)
Volga Partners · United States · US
Health Tech
Remote
Pharmacist
Demand65
Career growth60
Healthcare fit72
Remote potential90
Salary band
USD 20 – 50
5-year outlook
Likely remains project- or task-based supplemental income with variable rates depending on expertise and project availability. It is not a predictable full-time salary path unless it expands into broader AI evaluation or pharma consulting work.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
–
Date found
2026-10-26
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Freelance
- Hours
- Variable hours
- Eligible countries
- United States
- Profession fit
- Pharmacist
- Rate period
- Hourly
Why this was classified this way
- freelance
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering as flexible supplemental work for experienced pharma regulatory, quality, manufacturing, or CMC professionals curious about AI. Less suitable for clinicians without substantial pharma industry experience or those needing stable hours and income.
Who should apply
Pharmacists or physicians with CMC regulatory affairs, GMP/QA, QC/analytical development, validation, auditing, manufacturing/MSAT, or regulatory submission writing experience. Pharma/biotech professionals seeking task-based AI evaluation work should also consider it.
CV angle
Frame real pharmaceutical experience around regulatory frameworks, GMP/quality systems, CAPA and deviation management, CMC submissions/eCTD, analytical validation, audit/inspection readiness, and structured scientific review. Highlight evidence of evaluating complex documentation, identifying technical inaccuracies, and providing clear feedback; do not claim AI experience unless genuine.
Skills to highlight
- CMC regulatory affairs
- GMP compliance
- Quality assurance
- CAPA and deviation management
- CTD/eCTD Module 3 authoring
- Analytical method validation
- Regulatory audit and inspection readiness
- AI-generated content evaluation
Role summary
A freelance subject-matter expert role for experienced pharmaceutical and biotechnology professionals who review AI-generated regulatory, quality, manufacturing, and scientific content, identify inaccuracies, and provide structured expert feedback to improve AI model performance.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.