Pharmacovigilance & Medical Safety Expert
MedicineUnited StatesFull-timePosted Nov 14
Join a leading AI lab's cutting-edge GenAI team to be at the core of the AI revolution, where your expertise fuels the development of the most advanced Large Language Models.
Overview
Join a leading AI lab's cutting-edge GenAI team and help build foundational AI models from the ground up. We're seeking talented Pharmacovigilance and Medical Safety subject-matter experts (SMEs) from the pharmaceutical and biotech industry to bring deep drug safety expertise and elevate the quality of our AI training data. This is a full-time commitment of 40 hours per week.
This is a W-2 employment position with Cincinnatus LLC, with the opportunity to be placed at a leading AI Lab as part of their extended workforce.
Key Responsibilities
- Guide research and engineering teams to close knowledge gaps and improve AI model performance in pharmacovigilance, signal detection, benefit-risk assessment, and global safety reporting.
- Design challenging, realistic drug safety tasks, such as case causality assessments, signal evaluation scenarios, aggregate report questions and risk management problems, and write accurate, well-structured solutions.
- Evaluate AI model outputs on drug safety questions for accuracy against ICH E2 guidelines and FDA and EU GVP requirements, and provide clear, written feedback.
- Develop guidelines and detailed rubrics to assess causality reasoning, MedDRA coding judgment, and benefit-risk conclusions across tasks.
- Collaborate with other subject matter experts to ensure consistency and accuracy in training data.