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Global Oncology Regulatory Lead - Associate Director

Sumitomo Pharma, Boise, ID, United States


A global pharmaceutical company is seeking an Associate Director of Regulatory Affairs (Oncology) in Boise, Idaho. This role involves leading regulatory strategy for oncology products, managing submissions to health authorities, and ensuring compliance with global regulations. Candidates should have a Bachelor's degree in a related field and at least 7 years of relevant experience, including at least 4 years in regulatory affairs. A strong understanding of FDA regulations and oncology development is essential.
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