Join Altasciences as the Associate Director of Regulatory Affairs specializing in nonclinical development. You'll lead strategic regulatory guidance for drug development focused on pharmacology and toxicology. In this senior role, you'll oversee regulatory strategy for preclinical programs, ensuring the success of clinical applications and submissions.

With 8-10 years of experience in Regulatory Affairs, your expertise will shape nonclinical data packages, directly impacting the entry of small molecules and biologics into the market. Key Responsibilities:

- Provide strategic regulatory guidance on nonclinical programs
- Develop regulatory strategies for clinical trial applications
- Lead preparation and review of regulatory submissions
- Conduct gap analyses of nonclinical data packages
- Serve as a subject matter expert for health authority interactions

Requirements:

- PhD or MSc in Pharmacology or related field preferred
- 8-10+ years of regulatory experience
- Expertise in IND/CTA submissions and toxicology
- Robust understanding of global regulatory frameworks
- Leadership experience in mentoring regulatory professionals

Shape the future of drug development at Altasciences with your regulatory expertise.

📌 Regulatory Affairs Associate Director at Altasciences (Laval)
🏢 Altasciences
📍 Laval