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 submissions
- Review and prepare nonclinical submission materials critically
- Analyze nonclinical data for regulatory compliance and risks
- Support cross-team collaborations for aligned development
- Mentor junior regulatory staff and promote excellence Requirements:
- Doctorate or Master's degree in relevant scientific fields
- Over 8 years of experience in Regulatory Affairs
- Proven ability with nonclinical data in drug submissions
- Familiarity with global regulatory standards
- Strong analytical and communication skills Shape the future of drug development at Altasciences with your regulatory expertise.

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