- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. Summary: This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc member and ... Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads the development and maintenance of the CCDS, US and EU labeling, and manages… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. SummaryThis position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc member and ... Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads the development and maintenance of the CCDS, US and EU labeling, and manages… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diseases and immune disorders. Summary Responsible for managing the design, development , optimization and administration of global HCM Platforms and processes. This ... expertise across multiple HRMS applications, possessing deep understanding of HR business processes, and business systems requirements. Accountable for global… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary Leads the development and management of DSI's local and global Strategic PV Partnerships and ... management. Review contribute to revision of DSI contracts (eg development , license, distribution agreements)Manage, negotiate, and revise collaborative license… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …insights and intelligence to inform decision making & drives digitalization and business solutions to attain NNI goals. Finance, Insights & Enterprise Solutions ... maintaining our facilities and assuring the integrity and completeness of all business transactions. At Novo Nordisk, you will have the opportunity to build… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personal development . Are you ready? The Position The Associate Director , Communication Ops is responsible for driving cohesive messaging and effective internal ... strategic planning and counseling, executive/leadership communications, employee engagement programs, business and news writing, and communications measurement Expert… more
- Genmab (Plainsboro, NJ)
- …serious diseases. From our people who are caring, candid, and impact-driven to our business , which is innovative and rooted in science, we believe that being proudly ... is essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director , Global Regulatory Affairs, Regulatory Strategy to be a part of our Global… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …insights and intelligence to inform decision making & drives digitalization and business solutions to attain NNI goals. Finance, Insights & Enterprise Solutions ... maintaining our facilities and assuring the integrity and completeness of all business transactions. At Novo Nordisk, you will have the opportunity to build… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …insights and intelligence to inform decision making & drives digitalization and business solutions to attain NNI goals. Finance, Insights & Enterprise Solutions ... maintaining our facilities and assuring the integrity and completeness of all business transactions. At Novo Nordisk, you will have the opportunity to build… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …considers relevant input and guidance to other areas within NACD including Operations Director and TA Heads Analyze And Anticipate Business Needs: Utilizes ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...the planning, conduct and reporting of clinical trials. Ensures business needs are met through alignment of business… more
- Genmab (Plainsboro, NJ)
- …serious diseases. From our people who are caring, candid, and impact-driven to our business , which is innovative and rooted in science, we believe that being proudly ... authentic is essential to fulfilling our purpose.The Role The Director of US Medical Affairs Solid Tumors Strategy will...oncology solid tumor portfolio. The individual will lead the development and execution of the US Medical Affairs strategy… 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 ... people who are caring, candid, and impact-driven to our business , which is innovative and rooted in science, we...Regulatory Affairs (GRA) and will report to the Sr Director , Labeling, Policy and Intelligence. The position will be… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …needs of customers and align with research objectives Serving as an internal expert on clinical informatics tools development in support of organization-wide ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...you ready to make a difference? The Position The Director , Clinical Informatics in the Clinical Data Science &… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and optimization of organizational resource allocation. Relationships Reports into Clinical Development & Operations (CDO) Director /Associate Director . ... overall business objectives. Align on project strategy with Portfolio Director and TA heads Resource Management: Managing resources such as personnel, equipment,… more
- Merck & Co. (Rahway, NJ)
- …marketed Oncology medicines. Our Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire ... in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and Assist the Senior/Executive Director /AVP in… more
- Merck & Co. (Rahway, NJ)
- …Responsibilities include but are not limited to: Act as a subject matter expert in process development and characterization of engineered enzymes for ... Job Description Director - Fermentation Operation (P5) The Continuous &...lead a microbial fermentation operation team to support process development and characterization efforts for engineered enzymes. As part… more
- Merck & Co. (Rahway, NJ)
- … Director will manage the entire cycle of clinical development , including study design, placement, monitoring, analysis, regulatory reporting, and publication. ... in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects Obtain internal and external expert opinion on… more
- Merck & Co. (Rahway, NJ)
- …understanding of the strategic elements of drug development . As a subject matter expert , the Director within the QP2-IO Group will work closely with teams of ... Job DescriptionJob Description Director -QP2-IO We are seeking an experienced talented...quantitative framework to impact strategies and decisions of drug development teams. Primary Responsibilities: Serving as an expert… more
- Merck & Co. (Rahway, NJ)
- …is to provide strategic technology decisions that link investments and achieved business outcomes. Our goal is to offer strategic technology decision-making that ... connects investments and achieved business results. This focus allows the team to be...to engage on IT's largest programs to guide the development and identification of enterprise capabilities needed to support… more
- Merck & Co. (Rahway, NJ)
- …contractor quality and technical personnel and will partner with internal development teams on objectives utilizing external contractors including GMP qualification ... as well as the support of small and large molecule development programs.- - Key Responsibilities: Activities that this position would be responsible for include:… more
