Join Altasciences as an Associate Director specializing in nonclinical regulatory affairs. Lead cutting-edge drug therapies from preclinical stages to market entry.As a strategic leader, you will provide regulatory guidance for nonclinical development, ensuring compliance and scientific rigor for drug submissions. Collaborating closely with multidisciplinary teams, you will interpret complex data and craft clear regulatory strategies. This role significantly impacts the efficiency of drug progression into clinical trials.Key Responsibilities:Direct regulatory strategies for IND and CTA submissionsReview and prepare nonclinical submission materials criticallyAnalyze nonclinical data for regulatory compliance and risksSupport cross-team collaborations for aligned developmentMentor junior regulatory staff and promote excellenceRequirements:Doctorate or Master's degree in relevant scientific fieldsOver 8 years of experience in Regulatory AffairsProven ability with nonclinical data in drug submissionsFamiliarity with global regulatory standardsStrong analytical and communication skillsShape the future of drug development at Altasciences with your regulatory expertise.#J-18808-Ljbffr

📌 Regulatory Affairs Associate Director – Nonclinical Focus (Laval)
🏢 Altasciences
📍 Laval