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 developmentDevelop and execute regulatory strategies for IND and CTA applicationsLead preparation of regulatory submission sections for accuracyConduct gap analyses to identify and mitigate regulatory risksServe as expert during health authority interactionsRequirements:PhD or MSc in Pharmacology, Toxicology, or related field8–10+ years in Regulatory Affairs focused on nonclinical developmentExpertise in IND/CTA submissions and safety assessmentsStrong understanding of global regulatory frameworksExperience in medical writing for nonclinical dossiersBring your regulatory leadership and strategic vision to Altasciences and impact global health.#J-18808-Ljbffr

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