- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director , CMO Operation as part of the Global Manufacturing and ... desirable.Significant experience of proposal review, contract negotiation and independently managing CMO management is essential.Highly Organized, detail… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders. Summary The Payroll Head is responsible for leading and managing all aspects of Payroll for close to 2,000 employees and supporting the ... of a company poised for continued growth. These responsibilities will include management of all day-to-day payroll operations and activities for all US (multi-state)… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Summary Responsible for managing the design, development, optimization and administration of global HCM Platforms ... as the principal functional expert and advisor for implementation and ongoing management and maintenance of the Company's global HRIS system (ie, SAP… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Global Business Process Manager, Global DX is responsible ... involves aligning process improvement initiatives with strategic business goals, managing the global process landscape, and fostering collaboration across business… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …issues. Based on timelines or resources, may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU. Preparation of ... functional teams through all labeling discussions with the FDA/CHMP while ensuring management alignment. Strategizes and plans for FDA meetings as needed. Acts as… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …readiness, cutover planning and execution, and post-go-live supportAdvocate change management within CSPV department by assessing org impact, proactively ... required Experience Qualifications- 7+ years of experience specific to managing PV System Implementation and validation processes, database business configuration,… more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director , Global Regulatory Affairs, Regulatory Strategy to be a part ... submission strategy for the compound. You must have strong project management capabilities and will be responsible for planning, coordinating, and executing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …projects to ensure homogeneity within IT and supports oversight and management of integrations solution design, implementation strategy and requirements gathering, ... limited to Clinical Operations, Clinical Development, Biostatistics and Data Management , Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … management skills and quantitative analysis skills required. Experience managing a small team, including their professional development, is highly desired ... capabilities. We're responsible for regulating accounting, upholding workplace safety, managing our supply chain and sampling, supporting technological and data… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for professional and personal development. Are you ready? The Position The Associate Director , Communication Ops is responsible for driving cohesive messaging ... the P&O function. Relationships This position reports to the Director of People Operations and sits within the larger...mailboxes for key communications Operational Coordination Take charge of managing the mailbox for EE and P&O teams, working… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …development. Are you ready to maximize your potential with us? The Position The Associate Director , Data & Analytics Governance is responsible for the governance ... skills to ensure vision is maintained across various NNI functions. Relationships The Associate Director , Data & Analytics Governance reports to the Senior … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing relationships with internal stakeholders ... head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring...(SOWs). The AD will be responsible for providing supplier management support and oversight to the North America CMR… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personal 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 ... 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)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as a member ... including communication of regulatory risks and associated mitigation plans to management and other internal stakeholders Perform regulatory review of all clinical… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategic risk mitigation efforts in alignment with the E&C's risk assessment, management and mitigation program. The Business Partner is responsible for regularly ... business on impactful risk mitigation strategies. Relationships Reports to the Senior Director , E&C Business Partner. Coordinates with employees in the Ethics &… more
- Genmab (Plainsboro, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director , Key Accounts will shape, implement, and execute Key Account ... Genmab's first asset in hematology, EPKINLY. This critical role will report to the Director of Key Customer Strategy and be expected to work closely within the US… more
- Genmab (Plainsboro, NJ)
- …trial specific Clinical Trial Teams (CTT) to deliver clinical trials including managing the trial budget. The GCTM is accountable for trial deliverables and ... the CTM role too.ResponsibilitiesLead the Clinical Trial Team (CTT) and Trial Management (TM) teamDefine and align CTT goals collaboratively with the teamReview and… more
- Genmab (Plainsboro, NJ)
- …to fulfilling our purpose.The Role & DepartmentThe Associate Director , Vendor Management , will play a pivotal role in managing the relationships with the ... for the vendors, across multiple trials, ensuring consistent communication and management .Manage MSAs for certain suppliers: own and manage the Master Service… more
- Genmab (Plainsboro, NJ)
- …essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be responsible for leading the development ... will be within Global Regulatory Affairs (GRA) and will report to the Sr Director , Labeling, Policy and Intelligence. The position will be based in our Princeton,… more
- Merck & Co. (Rahway, NJ)
- …process development, qualification, and validation; and design control and risk management techniques to positively support and influence clinical and commercial ... engineering analysis and testing, medical device design controls, risk management , test method/fixture development, design verification and validation, injection… more
