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Associate Director, Clinical-Regulatory Methodology (Madrid)

Company

Cheiron

Location

madrid, comunidad de madrid

Type

Full-time

Company Overview

Cheiron is an AI-native pharma platform. Our products are in market today, supporting biopharma knowledge workers across discovery, translational, nonclinical, clinical, and regulatory work.We are building a unique platform for native representation of biopharma workflows – one that can represent the entire process of drug development as connected, versioned objects rather than a stack of disconnected documents.

About the Role

You will translate hands‑on pharma expertise into the workflow specs, evaluation criteria, and acceptance contracts that turn Cheiron’s AI products into something a buyer’s regulatory team can sign off on – and define what state must persist (claims, evidence, commitments, dispositions) so the next workflow downstream can trust it. For each in‑scope workflow you will decompose how the work actually gets done, define what a correct output looks like, write the test set that proves it, and articulate what the platform...

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