- 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 ... Job SummaryThis role is responsible for design and overseeing, coordinating, and managing activities related to the ongoing operation of modules in SuccessFactors on… 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 ... the successful execution of all operational components of a large-scale global clinical program using strong clinical project and program management, leadership,… 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 ... research areas centered around rare diseases and immune disorders. Summary: The Senior Director , Head of RBQM (Risk Based Quality Monitoring) sets the vision and… 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 ... areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management… 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 ... areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end delivery of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is ... expertise in managing many aspects of quality in an international, global context in a regulated health care environmentProven ability to work directly with… 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 ... of Clinical Trial Materials (CTM).ResponsibilitiesLead the authoring, revising, and managing the day-to-day activities associated with the Dose Preparation… 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 ... as well as other research areas centered around rare diseases and immune disorders.SummaryThe Director , Clinical Safety, will be a product safety lead or part of a… 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 ... this newly formed TA Oncology organization. This position will report to the Global Head of Late-Stage Oncology Development. This individual will play a central role… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …lead and manage skills and capabilities development initiatives for the Global Finance and Procurement organization and oversee project management for Finance, ... strong project management skills, this role will engage with diverse stakeholders across global teams. Work closely with project teams to ensure that changes are… 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 ... the Daiichi Sankyo US Business, and the Daiichi Sankyo Global IEP network.- Lead the design and execution of...achieving planned forecast spend, including but not limited to managing healthcare databases of claims and electronic health records… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAbout the Role:-As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a ... pivotal role in managing the technical interface between our company and our...ability to work independently. Proven leadership attributes including a global mindset, an end-to-end supply chain perspective, and strong… more
- Merck & Co. (Rahway, NJ)
- …the guidance of a senior leader, an Associate Principal Scientist/Associate Director , has primary responsibility for planning/ managing real world and ... development of American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers for use by local subsidiaries in their HTA submissions. The… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionReporting to the Executive Director , RIIM , this role will be accountable to ensure a holistic Regulatory centric D ata M anagement ( R DM) capability ... 2025 ( ie IDMP related activities and submissions to Global Health Authorities ) . Th is will result...c ross functional Leaders is critical. Th e Senior Director should have strong managerial experience, a high-level strategic… more
- Merck & Co. (Rahway, NJ)
- …SummaryUnder the guidance of a senior leader, a Principal Scientist/ Director , has primary responsibility for developing value evidence strategies, and ... planning/ managing real world and economic evidence activities for cross...Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers for use by local subsidiaries in… more
- Merck & Co. (Rahway, NJ)
- …DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company ... priorities. - Detail Oriented & Organized:- strong attention to detail in managing complex supply chain activities;- ability to multitask, prioritize tasks, and meet… more
- Eisai, Inc (Nutley, NJ)
- …essential. Demonstrated track record of interfacing effectively with FDA, EMA and other global regulatory agencies. Experience in managing the preparation of a ... is your profile, we want to hear from you. Job Summary The Executive Director , Regulatory Affairs will provide leadership and direction for the global regulatory… more
- Eisai, Inc (Nutley, NJ)
- …project managers, line managers, clients and other stakeholders.Job Summary:The Associate Director , Global Alzheimer's Disease Project Management is responsible ... for facilitating the operational aspects of the lecanemab global launch plan, provide project management, and serve as liaison between project team, global team,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharma/biotech/medical device industry - Required 4+ years of proven leadership experience managing technical and validation teams, preferably at Director or ... 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
- Formation Bio (New York, NY)
- …and more efficiently.About the PositionAs Formation Bio's dedicated IP Counsel at the Director level, you will own the IP function for our rapidly growing pharma ... company. Reporting to the Senior Director , you will operate autonomously to create and execute...our IP operations to align with business growth. Oversee global patent prosecution, trademark registrations, and related payments. Manage,… more
