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The Executive Medical Director, (SERM) will be responsible for leadership of a program(s) within the Risk Management & Pharmacovigilance Department.
The Head of Medical Affairs leads a 60 person Medical Affairs function in support of all approved and late-stage development compounds.
The Sr. Medical Dir. will serve as a scientific and medical expert for the MA dept. at Seattle Genetics, as well as other groups across the company.
The Associate Medical Director will be responsible for developing and implementing the life cycle strategy of brentuximab vedotin.
The Medical Director will be responsible for developing and implementing the life cycle strategy of brentuximab vedotin.
The ADCETRIS Global Development Leader (GDL) leads the development of ADCETRIS and other CD30 directed therapies.