We are seeking an experienced Associate Director for our Global Regulatory Affairs team within our Life Sciences Division. The successful candidate will have a proven track record on filing and liaising with regulatory authorities, specifically the US Food and Drug Administration and European Medicines Agency including Medicines & Healthcare Products Regulatory Agency of the United Kingdom. Experience in Oncology or new therapeutic modalities is preferred. As the Associate Director, you will provide expert guidance in the following key areas:
The ideal candidate will have:
The position requires flexible working hours, with the ability to travel (international or domestic), and the expectation to be office-based when not travelling.
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