The Director of RA CMC will provide strategic management and leadership to support the Regeneron portfolio of products assigned. Specifically, this new role will include CMC regulatory leadership on gene therapy products. The candidate will be responsible for assuring development and execution of regulatory strategies for drug products and combination products in the US & EU and lead the activities of other CMC regulatory affairs staff or contract regulatory support in the performance of the duties outlined below.
In this role, a typical day might include the following:
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