Daiichi Sankyo US
Pharmaceuticals
Daiichi Sankyo US is a pharmaceutical company with a rich history of innovation and excellence in drug development. With its U. S. headquarters in Basking Ridge, New Jersey, the company focuses on marketing, medical affairs, sales operations, and clinical trial support. Daiichi Sankyo is dedicated to groundbreaking science and fostering a culture of learning and growth, providing comprehensive healthcare benefits and extensive training and education resources. As an industry leader, their commitment is reflected in their approach to employee development and inclusion.
10,000+ employees
Founded 2005
💊 Pharmaceuticals
Director, US Regulatory Intelligence – Policy Lead
Job not on LinkedIn
October 11
Daiichi Sankyo US
Pharmaceuticals
Daiichi Sankyo US is a pharmaceutical company with a rich history of innovation and excellence in drug development. With its U. S. headquarters in Basking Ridge, New Jersey, the company focuses on marketing, medical affairs, sales operations, and clinical trial support. Daiichi Sankyo is dedicated to groundbreaking science and fostering a culture of learning and growth, providing comprehensive healthcare benefits and extensive training and education resources. As an industry leader, their commitment is reflected in their approach to employee development and inclusion.
10,000+ employees
Founded 2005
💊 Pharmaceuticals
📋 Description
• Lead US regulatory intelligence acquisition, analysis, communication, and knowledge management • Interpret and apply US regulatory intelligence to inform strategic decisions • Manage and improve the GRIP CoE Hub • Develop and implement an assigned project portfolio • Lead DS regulatory policy and advocacy activities for assigned topics
🎯 Requirements
• Bachelor's degree in medicine, life sciences, health, or related field required • 7 or more years' experience in biopharma Regulatory Affairs • At least 3 years developing regulatory strategies • 4 or more years leading Regulatory Intelligence & Policy activities in the U.S. • Strong relationships across FDA and PhRMA highly desirable • 1 or more years experience working with international teams • 1 or more years experience of working with oncology drugs, Biologics/ADCs Companion diagnostics preferred
🏖️ Benefits
• Exceptional working environment • Training and tools provided • Open communication • Emphasis on results • Spirit of personal accountability
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