Lead nonclinical regulatory strategies at Altasciences as an Associate Director. Drive successful drug development efforts through expertise in pharmacology and toxicology. In this senior regulatory role, you will guide the regulatory strategy for preclinical programs, ensuring a robust nonclinical data package for clinical trials.

You will collaborate with cross-functional teams and sponsors to translate complex scientific data into regulatory strategies. Your contributions will enhance the entry of small molecules and biologics into the clinic. Key Responsibilities:
Provide strategic regulatory guidance on nonclinical drug development
Develop and execute regulatory strategies for IND and CTA applications
Lead preparation of regulatory submission sections for accuracy




Conduct gap analyses to identify and mitigate regulatory risks
Serve as expert during health authority interactions Requirements:
PhD or MSc in Pharmacology, Toxicology, or related field
8–10+ years in Regulatory Affairs focused on nonclinical development
Expertise in IND/CTA submissions and safety assessments
Robust understanding of global regulatory frameworks
Experience in medical writing for nonclinical dossiers Bring your regulatory leadership and strategic vision to Altasciences and impact global health.

📌 Associate Director Of Regulatory Affairs At Altasciences Laval (Canada)
🏢 220 Altasciences
📍 Canada