- Merck & Co. (Rahway, NJ)
- …Research & Division organization of our company. - Position Description/Summary: - The GPAM Associate Director , Project Manager, is a core member of Early ... 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
- Genmab (Plainsboro, NJ)
- …to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be responsible for leading the development and ... maintenance of global labeling documents (eg, Core Data Sheet, USPI, EU...Regulatory Affairs (GRA) and will report to the Sr Director , Labeling, Policy and Intelligence. The position will be… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as ... preferred Minimum of 8 years total pharmaceutical/related industry experience in drug development required Demonstrated knowledge of global regulatory… more
- Merck & Co. (Rahway, NJ)
- …the R&D engine that drives our Company's biopharmaceutical business.Position Description: Associate Director , Finance Clinical Development Finance (CDF) is ... and individual goals.Under the guidance of the Oncology Clinical Development Finance Director , the Finance Associate Director will:Provide financial… more
- Genmab (Plainsboro, NJ)
- …be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical development ... as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent, ... actionable insights to guide the business. Relationships Reports to the Director , MAPA Insights. Internal relationships include close interactions with Market Access… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director of In Vivo Pharmacology as part of the Research & ... Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one...mice and NHPAssess safety and tox risks of cell-based drug productsAnalyze, document and report all experiment findingsPerform additional… more
- Merck & Co. (Rahway, NJ)
- …Under the direction of the Program Lead, you will collaborate with global , cross-functional team members including clinical directors and study managers to ... clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct/indirect team members through… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …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 ... and management to drive strategies and activities for early and late phase drug development candidates within the team to support overall CMC development plan.-… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... teams for the diagnostic, under the direction of the Global Program Teams (GPT) CDx representative for the therapeutic...assay technologies such as NGS, IHC, PCR etc.Knowledge of drug development process and an understanding of how diagnostic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …not limited to briefing documents, breakthrough therapy designation requests, orphan drug applications.Participate in global product team meetings (development ... 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)
- …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 ... with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted… more
- Eisai, Inc (Raleigh, NC)
- … global GxP and regulatory requirements related to the drug development process.Significant experience with manufacturing operations, biologics, and aseptic ... manufacturing.Experience with highly automated parenteral manufacturing processes, including isolators, automated inspection, Manufacturing Execution Systems and electronic batch release.Competent in analyzing complex products, production, and testing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. Our Research ... and an inspiring mission to achieve new milestones in global healthcare. The Biologics and Biopharmaceutics team is responsible...for the research and development of sterile & parenteral drug products for biologics as well as the biopharmaceutics… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential Functions Innovation and ... or a life sciences/pharmacy nursing degree with 15+ years' experience in global safety surveillance and/or clinical/ drug development Excellent verbal and written… more
- Genmab (Plainsboro, NJ)
- …essential to fulfilling our purpose.The Role & Department As a Senior Programming Associate or Programming Manager, you will be in the Statistical Programming team ... making and reporting to health authorities. You will report to the Director , Programming, and work closely with Data Management, Clinical Programming, Statistics,… more
- Boehringer Ingelheim (Ridgefield, CT)
- …impact on patients' lives? Boehringer Ingelheim is seeking a dedicated and innovative Director /Senior Associate Director , Global Regulatory Affairs CMC ... CMC Director or Senior Associate Director has responsibility for the strategic global ...without restriction. + Must be willing to take a drug test and post-offer physical (if required). + Must… 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...field as applicable. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Lead, GI & Inflammation where you ... will define, develop, and lead global strategies to maximize global regulatory success...field as applicable. **How you will contribute:** + The Associate Director will be responsible for complex… more
- Merck (North Wales, PA)
- …Research & Division organization of our company. ** ** **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early ... 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
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