Elevate nonclinical drug development strategies with Altasciences as an Associate Director of Regulatory Affairs. This pivotal role focuses on regulatory compliance for clinical submissions and pharmacology. You will work collaboratively with cross-functional teams, translating complex nonclinical data into actionable regulatory strategies. Your background of 8-10 years in Regulatory Affairs will be essential in guiding compliance and ensuring rigorous preparation of submissions such as IND and CTA. Key Responsibilities:
- Guide regulatory strategy for pharmacology and toxicology studies
- Prepare and critically review regulatory documentation
- Conduct risk assessments of nonclinical data
- Collaborate with clinical, toxicology, and writing teams
- Mentor junior regulatory staff to achieve excellence Requirements:
- PhD or MSc in relevant discipline preferred
- Over 8 years of experience in regulatory affairs
- Knowledge of global regulatory requirements
- Proven ability in medical writing and dossier preparation
- Robust analytical and project management skills Drive innovation in drug development at Altasciences, leveraging your regulatory experience. #J-18808-Ljbffr

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