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Associate Director of Regulatory Affairs - Pharmaceuticals

Randstad Life Sciences US
Nashville, TN Full Time
POSTED ON 3/19/2025
AVAILABLE BEFORE 4/17/2025

If you are an Associate Director Level Regulatory Affairs Professional with an interest in moving to Nashville and working for a Small Pharma client where your input will be heard, then check this out.

Associate Director (ideal for a Senior Manager looking for a jump in title)

140k-150k salary 20% bonus

Relocation Package

We are seeking experience with :

Ad Promo

Experience dealing with the FDA

Annual reports, submissions, writing, labeling

A passion for collaboration

5-10 years of Regulatory experience in Pharma

In this role you will :

Bring oversight of the Company’s regulatory activities, including the design and implementation of clinical studies and preparation of pre-approval and post-approval regulatory submissions.

Participate in the preparation and review of a variety of regulatory documents, including NDA, INDs, and their amendments and supplements.

Assist with the preparation and review of Annual Reports for the Company’s approved brands and investigational candidates.

Being a small company, work on the Ad Promo side of Regulatory as well.

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