- Merck & Co. (Upper Gwynedd, PA)
- … and regional directors and associate directors. The EDMA engages with global scientific leaders and key decision makers. The EDMA partners with Product ... Job DescriptionThe Executive Director , Global Medical and Scientific Affairs (EDMA) GYN Malignancies is accountable for the development and execution of … more
- Merck (Honolulu, HI)
- … and regional directors and associate directors. The EDMA engages with global scientific leaders and key decision makers. The EDMA partners with Product ... Merck Executive Director , Global Medical and Scientific Affairs, GYN Malignancies Honolulu, Hawaii Apply NowThe Executive Director , Global Medical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary A key part of the Global HR team, the Associate Director of Global HR ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...development and execution of strategic change communication plans. The Associate Director will contribute to the development… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Strategic Planning provides strategic ... science and technology. With more than 120 years of scientific expertise and a presence in more than 20...diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 120 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for execution of global scientific and training deliverables. The Associate Director develops and executes Medical Content and Training plans and works ... science and technology. With more than 120 years of scientific expertise and a presence in more than 20...areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Global Medical Affairs… more
- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide.As an Associate Director , Global Regulatory Affairs Marketed Products you will ... define, develop and lead global strategies to maximize global regulatory success...and influencing the field as applicable.How you will contribute:The Associate Director will be responsible for increasingly… more
- ClickJobs.io (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. As an Associate Director , Global Regulatory Affairs Marketed Products you will ... define, develop and lead global strategies to maximize global regulatory success...the field as applicable. How you will contribute: The Associate Director will be responsible for increasingly… more
- Takeda (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide.As an Associate Director , Global Regulatory Affairs Marketed Products you will ... define, develop and lead global strategies to maximize global regulatory success...and influencing the field as applicable.How you will contribute:The Associate Director will be responsible for increasingly… more
- Takeda Pharmaceutical (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. As an Associate Director , Global Regulatory Affairs Marketed Products you will ... define, develop and lead global strategies to maximize global regulatory success...the field as applicable. How you will contribute: The Associate Director will be responsible for increasingly… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for ... science and technology. With more than 120 years of scientific expertise and a presence in more than 20...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders.Summary The Associate Director of Regulatory Writing is a key role responsible for ... science and technology. With more than 125 years of scientific expertise and a presence in more than 20...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director , Program Management is a senior position responsible for ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...as achieving overall project level quality metrics. An ideal Associate Director , Program Management must have the… more
- Merck & Co. (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... standards and policies and business objectives.Actively participate in labeling and global regulatory team meetings to ensure support for anticipated promotional… more
- Merck & Co. (North Wales, PA)
- …the Research & Division organization of our company.- Position Description/Summary: The GPAM Associate Director , Project Manager, is a core member of Early Drug ... Job DescriptionThe drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in...& Development pipeline and realize its full potential. The Associate Director is expected to provide project… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director of Quality Project Management and Strategyas part of the ... Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one...Quality team based in Raritan, NJ. Role OverviewThe Associate Director of Quality Project Management and… more
- AstraZeneca GmbH (Boston, MA)
- This is what you will do:Position SummaryThe Associate Director of Global Regulatory Affairs Chemistry, Manufacturing, and Controls (GRA-CMC) will be ... responsible for leading and providing global CMC regulatory support for the clinical and commercial...Manufacture, also considered.Education: BA/BS degree (or equivalent) in a scientific discipline, MS or Ph.D. preferred.Strong written and oral… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development ... Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one...cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo… more
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