Associate Director, US Regulatory Affairs: ON-Hamilton, Major Responsibilities 1.Effectively develops strategic regulatory plans for client drug development programs. 2.Plans and prepares all submission types (e.g. CTA, IND, NDA, Annual Reports, expedited safety reports, etc) to regulatory authorities in adherence with applicable Acts, Regulations and Guidance for submission to government agencies (focus on FDA). 3.Facilitates submission approvals thro

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