
Global Oncology Regulatory Lead - Associate Director
Sumitomo Pharma, Lincoln, NE, United States
A global pharmaceutical company is seeking an experienced Associate Director of Regulatory Affairs to lead regional regulatory activities focused on oncology products. The role involves preparing regulatory submissions, developing strategies, and ensuring compliance with health authority requirements. Candidates must have at least 7 years of biopharmaceutical experience, with 4+ years in regulatory affairs, and a bachelor's degree in a related field. This position offers a competitive salary range of $156,000 to $195,000 along with a robust benefits package.
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