- 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 ... and provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of BLA/MAA… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …internal controls and documented procedures are created and followed. Benchmark process by developing and maintaining payroll measurements and scorecards. Performs ... transaction error analysis and initiates best practices and process improvement activities were warranted.Functions as the primary contact for interactions with the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …well as other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Global Business Process Manager, Global DX is ... to ensure effective transformation and automation across the organization. Responsibilities Process Design, Development , and Optimization:- Coordinate and lead… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. Summary This position works with the Director , Clinical Study Startup to establish the strategy driving global Clinical Study ... decisions where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong organization and interpersonal… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Reinforces labeling best practices at cross-functional meetings. Assists in the development of Standard Operating Procedures (SOPs) and process improvements. ... including post marketing projects and those involving 3rd party development . This position partners with GRLs and Clinical Safety...may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …preferred- 4 or More Years Extensive experience in project management, process , product, and/or analytical development activities and pharmaceutical/oncology ... defined based on the project needs and the respective development stage of the project. The CMC Lead will...Participate in cross-functional teams responsible for regional and global process improvements in the operational efficiency of PJ Lead… more
- Merck & Co. (Rahway, NJ)
- …the Research & Development pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive ... of our company. - Position Description/Summary: - The GPAM Associate Director , Project Manager, is a core...Director is expected to contribute to ongoing business process improvement and talent development in Global… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and technical feasibility and delivery. The role supports all phases of systems development for global informatics systems, ETL and integrations. The Tech Lead must ... include but are not limited to Clinical Operations, Clinical Development , Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …implement effective regulatory strategies to deliver on efficient and robust development plans. The individual will direct, coordinate and implement the preparation ... regulatory agencies receive timely and quality submissions, shortening the review process and leading to successful approval of pharmaceutical applications for the… more
- Merck & Co. (Rahway, NJ)
- …Description Position Description: The Office of General Counsel is seeking an Associate Director , Trademark Operations to provide docketing and legal operations ... & Copyrights group to develop and enforce best practices and process improvements; and lead and manage strategic projects, including assignment recordation… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …alternate solutions and provide technical recommendations for Changes and process improvements.Provide oversight, Manage Implementation and documentation of PV ... ensuring the design of the CSPV solution that satisfies the business process visionLead platforms and systems design and optimization to deliver best-in-class… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... on a continuous basis in decision making and driving pipeline impact. The Associate Director will perform job duties independently with minimal supervision… more
- Merck & Co. (Rahway, NJ)
- …financial evaluation, and business development activity for their business area.-The Associate Director is part of a team that partners closely with ... Job DescriptionThe Associate Director is a member of...Neuroscience Portfolio including alliance support, profit/cost sharing and business development modeling.- Within HIV, this role will be responsible… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur company's Device Product & Process Development (DPPD) Team designs, develops, and commercializes novel biologic/drug/vaccine - device enabled ... position will be responsible for applying their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to… more
- Merck & Co. (Rahway, NJ)
- …build and lead a team of TA dedicated global and regional directors and associate directors. The Executive Director , Value & Implementation (referred to as EDMA) ... Job DescriptionThe Executive Director , Value & Implementation (V&I), Global Medical and...V&I Outcomes ResearchSupports the Investigator-Initiated Study programLeads talent review process and demonstrates follow-through on Development Plans… more
- Merck & Co. (Rahway, NJ)
- …healthcare. The Biologics and Biopharmaceutics team is responsible for the research and development of sterile & parenteral drug products for biologics as well as ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … development . Are you ready to maximize your potential with us? The Position The Associate Director will be the lead who is responsible for ensuring that all ... Reports to the Sr. Director , Patient Support Solution Quality/Safety Associate Director . Interacts with colleagues within Patient Support Programs, Patient… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …. Are you ready to maximize your potential with us? The Position The Associate Director , Data & Analytics Governance is responsible for the governance of ... vision is maintained across various NNI functions. Relationships The Associate Director , Data & Analytics Governance reports...budget activities required We commit to an inclusive recruitment process and equality of opportunity for all our job… more
- Insmed Incorporated (New York, NY)
- …and ancillary healthcare professionals regarding current and future therapies in development or commercialized by Insmed Works closely with Insmed personnel to ... and deliver HCP derived scientific insights to Insmed.Support research and development programs as requested by R&D, Clinical Operations, and Medical Affairs… more
