Clinical Pharmacology Consultant
About The Position
Edison Scientific builds and deploys AI scientist agents to accelerate science and the development of new medicines. We are an ambitious team run by scientists and engineers from leading institutions across biology, physics, chemistry, and AI. We're seeking an experienced Clinical Pharmacology domain expert for a flexible, part-time consulting engagement. You'll serve as the scientific voice on human PK/PD, defining what correct looks like for AI-generated clinical pharmacology outputs, and ensuring our platform produces results that would hold up in a regulatory submission. This is an ad-hoc opportunity designed to fit around existing commitments. This engagement will likely be 5-20 hours per week and is ad-hoc in nature.
Requirements
- 10+ years of experience in clinical pharmacology, preferably at a sponsor
- PhD, PharmD, or MD preferred
- Hands-on experience with exposure-response and population PK analyses included in regulatory submissions
- Experience authoring or reviewing clinical pharmacology sections of INDs, IBs, CSRs, and NDA/BLA modules
- Direct experience responding to regulatory agencies
- Enthusiastic about working with AI tools to evaluate and improve outputs
Responsibilities
- Knowledge sharing about "day-in-the-life" as an expert working with data in these domains to assemble regulatory submissions.
- Describing common tasks or problems where AI could be of value in your workflows.
- Identify + describe internal pharma systems that are commonly used for standard workflows.
- Generate or review reference ground-truth artifacts to evaluate against - reports, data files, modules, etc.
- Identify + add realistic sources of variance or data corruption in study data.
- Identify and correct discrepancies in data quality.
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What This Job Offers
Job Type
Part-time
Career Level
Senior
Education Level
Ph.D. or professional degree
