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Test and validate Ather AI conversations for medical accuracy, clinical relevance, and compliance, using approved references and scientific literature. Create gold-standard Q&A sets and test cases, flag inaccuracies and safety risks, and collaborate with medical, product, and engineering teams to improve AI outputs.
Overview
We are looking for a Part-Time Medical Information Associate / MSL to support testing and medical validation for our Ather product line. This role is critical to ensuring our AI medical experts are clinically accurate, medically relevant, and 100% compliant.
You will work closely with Product, Engineering, and Medical Affairs to test conversational AI outputs, review medical information accuracy, create gold-standard responses, and flag compliance risks. This is a flexible, part-time role ideal for someone with a strong medical/pharma background who wants exposure to cutting-edge AI in life sciences.
Responsibilities
Medical Accuracy & Product Testing
Test Ather product conversations for medical accuracy, clinical relevance, and tone for HCPs.
Review and validate AI-generated responses against approved medical references, PI, and scientific literature.
Create and maintain gold-standard Q&A sets, test scripts, and edge cases for medical information queries.
Identify and document medical inaccuracies, hallucinations, and compliance risks.
Compliance & Quality
Ensure all responses adhere to medical-legal-regulatory (MLR) standards and pharma compliance guidelines.
Flag adverse events, off-label queries, and product complaints as per pharmacovigilance SOPs.
Collaborate with medical team to define guardrails and approval criteria for AI outputs.
Cross-Functional Collaboration
Work directly with product and engineering teams to provide medical feedback and improve model performance.
Translate complex medical queries into structured test cases and evaluation criteria.
Contribute to medical knowledge base and content curation for Synthio products
Qualifications
Education
Advanced degree in Life Sciences - PharmD, MBBS, BDS, M.Pharm, M.Sc Pharmacology / Life Sciences, or equivalent. MSL / Medical Information background preferred.
Experience
3-5 years of experience as Medical Information Associate, MSL, Medical Affairs Associate, or Medical Reviewer in pharma / healthcare.
Strong understanding of medical information workflows, MLR review, and pharma compliance.
Experience in literature search, fact-checking medical content, and referencing (PubMed, package inserts, etc.).
Familiarity with AI tools, LLMs, and prompt evaluation is a strong plus.
Skills
Excellent attention to detail and critical thinking for medical accuracy.
Strong written communication - ability to write clear, HCP-friendly medical responses.
Comfort working in a fast-paced, early-stage startup environment with flexible hours.
Ability to work independently, 15-20 hrs/week, with overlap with US hours as needed.
What Makes This Role Unique
Directly shape the safety and accuracy of AI medical experts used by real pharma teams.
Blend medical affairs expertise with cutting-edge AI product testing.
Flexible, part-time, remote role with high ownership and direct access to founders and product team.
Be part of building the next generation of compliant AI for life sciences from 0 to 1.
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Marketing Manager
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