Ready to have an impact? Sumitomo Pharma Oncology, Inc. (SMP Oncology) is hiring for the following positions.
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Associate Director, Pharmacovigilance Scientist
We are seeking an experienced Associate Director, Pharmacovigilance Scientist to join the Drug Safety and Pharmacovigilance team. In this exciting and challenging role, you will work collaboratively with the Program Safety Lead and other PV Scientists and Physicians and play a leading role in performing PV activities for your assigned drug project(s). You may also have the opportunity to work as a Program Safety Lead, depending on your prior experience. Your ability to work collaboratively will facilitate cross-functional engagement with colleagues from across the organization including, but not limited to, Clinical Development, Regulatory Affairs, and Biostatistics.
Associate Medical Director, Drug Safety and Pharmacovigilance
The Associate Medical Director will provide hands-on PV support for SMP Oncology investigational and commercial stage oncology products. Responsibilities include routine PV surveillance, data assessment for aggregate safety reporting, and maintenance of the benefit/risk profile in a cross-functional team environment. There will be opportunities to provide PV subject matter expertise to clinical development activities such as updating program clinical study documents (e.g., protocols and Investigatorâ€™s Brochures) and writing Clinical Study Reports. Additionally, this person will be responsible for performance of Medical Review with support from an external partner.
Director, Field Medical and Scientific Affairs - East
The Director, Field Medical and Scientific Affairs will be responsible for integrating scientific expertise and knowledge with brand strategies to ensure successful implementation of the Company's emerging product portfolio. This position leads, directs, coordinates, and supports the activities of the Field Medical Science Liaisons within the specified region to achieve clinical and business objectives. This position works cross-functionally to identify, develop, and implement field MSL training, strategies, and tactics. The incumbent will help drive the Thought Leader strategy, ensuring the company is effectively positioned for developing advocates.
Senior Manager, PV Scientist and Study Lead
The Senior Manager, Pharmacovigilance Scientist and PV Study Lead will play a leading role in performing PV activities for your assigned drug programs(s). This individual will work collaboratively and will facilitate cross-functional engagement with colleagues from across the SMP Oncology organization including, but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics.
Vice President, Head of Clinical Development
The Vice President, Head of Clinical Development will be responsible for leading the clinical development activities for assigned clinical program(s) within a matrixed environment and provide subject matter expertise and direction to the development and operations of assigned clinical project(s).
Vice President, Medical and Scientific Affairs
The Vice President, Head of Medical and Scientific Affairs will be responsible for the strategic development, execution and management of scientific and medical information for key stakeholders. The Vice President will lead the global medical affairs functions for investigational and marketed products.