Altasciences in Quebec, Canada seeks an Associate Director of Regulatory Affairs – Nonclinical Development to lead regulatory strategy for preclinical programs across pharmacology, toxicology and ADME. You will guide IND/CTA submissions and partner with cross‐functional teams to translate complex nonclinical data into explicit regulatory plans.You will mentor regulatory and scientific staff, support business development, and ensure compliance with GLP, GMP and GCP standards while engaging with #J-18808-Ljbffr
📌 Nonclinical Regulatory Affairs Lead – Associate Director (Montreal)
🏢 Altasciences
📍 Montreal
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