- Genmab (Plainsboro, NJ)
- …is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director, Global Clinical Drug Supply to be part of Global Clinical ... the planning of operational excellence, strategic planning, and innovation implementation for the Global Clinical Drug Supply team. The individual will have the… more
- Genmab (Plainsboro, NJ)
- …to fulfilling our purpose.The Role & DepartmentGenmab is seeking an experienced Senior Clinical Drug Supply Manager to join our Global Clinical Drug Supply ... packaging and labeling clinical trial supplies, collaborating closely with the Global Clinical Drug Supply Planning team. Together with the Global Clinical… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.Genmab is seeking a Clinical Drug Supply Manager to join our Global Clinical Drug Supply ... locations to work according to our hybrid work arrangement.Responsibilities/tasks:Act as Clinical Drug Supply Manager, of the following tasks: Global Clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …zones such as Japan. Education/Experience: o Express an interest in Leadership and Global Research and Development Drug Processes. Prior experience in project ... 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
- Genmab (NJ)
- …the CSR Attend trial and investigator meetings if/as needed Collaboration with Genmab Global Drug Safety:Participate in definition, review, and approval of data ... scientific and technical progress within the field of biostatistics in drug development and advise of new methodologies that may support innovation… more
- Merck & Co. (Rahway, NJ)
- Job Description Overview: The Director, Global Media Relations, is responsible for developing and executing a global media strategy that showcases our Company's ... mainstream and consumer reporters and editors within the US and across key global markets. To support our Company's media relations efforts, this individual will… 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 ... and immune disorders. Summary: Responsible for leading and developing global regulatory strategy for assigned development projects. Represents Daiichi Sankyo's… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential 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 SmPC and related patient information) for the Genmab portfolio of… more
- Merck & Co. (Rahway, NJ)
- …Job Description: - The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & Division ... - The GPAM Associate Director, Project Manager, is a core member of Early Drug Development and/or Late Drug Development Teams, partnering with team leaders to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Respiratory will focus on driving strategy, development, and life-cycle ... understanding of the disease area, the functions and processes relevant to drug development, and project management principles as applicable to the pharmaceutical… more
- Merck & Co. (Rahway, NJ)
- …Section Head in the Atherosclerosis & Metabolism Therapeutic Area within Global Clinical Development will focus on driving strategy, development, and life-cycle ... of the disease area, the functions and processes relevant to drug development, and project management principles applicable to the pharmaceutical industry.Primary… more
- Genmab (Plainsboro, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of a ... to CPL in a timely mannerExecute operational strategies related to drug supply, regulatory submissions, and recruitmentBudget and PlanningAssist in the initial… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …document. May participate in meeting or teleconferences with Health Authorities- Global BDO Strategy to Improve Drug Development: Primarily participates ... 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
- Merck & Co. (Rahway, NJ)
- …materials characterization tools and techniquesExtensive knowledge of technical and global regulatory requirements for medical devices and combination products, ... including FDA, EU MDR, ISO, and other applicable guidelines.-Excellent communication, negotiation, interpersonal skills, and problem-solving skills, with the ability to effectively engage with internal and external stakeholders and industry partners.Strong… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …senior representative with key high-level internal and external stakeholders on important drug safety issues supporting Global Medical Safety Lead. Responsible ... 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)
- …not limited to briefing documents, breakthrough therapy designation requests, orphan drug applications.Participate in global project 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)
- …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)
- …partners to ensure high quality coding deliverables are on time to support drug development processes and global submissions. This position also partners with ... 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)
- …with CROs and other vendors to ensure high quality deliverables to support drug development processes and global submissions as required for clinical trials. ... 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)
- … drug listing, track and archive affiliate labeling for global products and review proposed labeling from affiliates. Responsibilities Provide Regulatory ... 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
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