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Associate Director, Regulatory Affairs – Nonclinical Development at Altasciences - ApplyBlast

Associate Director, Regulatory Affairs – Nonclinical Development

Altasciences

3 months ago

3.0 on Glassdoor

Columbia, Missouri, United States

Onsite

Full Time

Director

0 applicants

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About this role

The Associate Director, Regulatory Affairs – Nonclinical Development leads strategic regulatory planning for preclinical programs, ensuring nonclinical data packages support successful clinical entry and market submissions. This role partners with sponsors and cross‑functional teams to translate complex pharmacology, toxicology, and ADME data into clear regulatory strategies and submission‑ready documentation.

Responsibilities

Provide strategic regulatory guidance for nonclinical development programs
Lead preparation and critical review of nonclinical sections of regulatory submissions
Mentor and guide junior regulatory professionals

Skills

Qualifications

PhD in Pharmacology, Toxicology, Pharmaceutical Sciences or related disciplineMSc in Pharmacology, Toxicology, Pharmaceutical Sciences or related discipline

About Altasciences

altasciences.com

Headquarters

Laval, Quebec, Canada

Company Size

1001-5000 employees

Founded

1995

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Contract research organization specialized in seamless, end-to-end, early phase drug development, we act to get your most promising compounds into and through early phase clinical trials.