- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US Product Team to inform clinical development , commercialization, market access, and ... for assigned compound under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical Affairs (USOMA). Develops… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of Medical Affairs QA is ... across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director , Global Oncology Medical Affairs, Medical Analytics will be responsible for ... teams.Responsibilities- Data-Driven Insights Reporting and trend analytics: Lead the development and implementation of robust analytics frameworks, Gen-AI and NLP… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Summary: The Sr. Director , Clinical Safety MD, will lead the development and implementation of integrated project/ product risk management strategies aimed at ... assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development , Regulatory, Project Management,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …forums including, Publications Planning, Clinical and Safety sub-teams, and Global Product Team to inform clinical development , commercialization, market access, ... execution of the activities in the GMA plan.Responsibilities- Responsible for the development of the Global Medical Affairs early strategy and medical objectives for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the daily ... the signal workflow to ensure compliance with procedural documents.When required, assist the product safety teams in the entering of key signal information into the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Summary: The Oncology Clinical Educator role provides disease state, REMS, and product safety education and training to key healthcare providers within Oncology ... within a specified region to enhance disease, REMS, and product safety knowledge, coordinate and provide staff training, and...nurses working under the general direction of the Regional Director of Clinical Nurse Managers. The OCE is responsible… more
- Merck & Co. (Rahway, NJ)
- …activities. Additionally, this position will require applying knowledge in drug and device product development , such as manufacturing process development and ... Mechanical Engineering (or an equivalent field) + 8 years of combination product development experience; MS in Mechanical Engineering (or an equivalent field) +… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …execute daily production schedules.Will have 3-6 direct reports ranging from Associate Director , Senior Manager, and Manager.Oversee the hiring, development , and ... in the treatment of multiple myeloma.Legend Biotech is seeking Director of Operations as part of the Technical Operations...within the facility to ensure high quality and compliant product supply and oversee production metrics; these metrics will… more
- Merck & Co. (Rahway, NJ)
- …year attainment of brand operating metrics. The VCM PL will partner with the Product Development Team (PDT), Development and Commercialization Team (DCT), ... Finance, Regulatory, Quality, Compliance, Supply Chain and Commercial. Understanding of product development lifecycle and integration of CMC and clinical… more
- Merck & Co. (Rahway, NJ)
- …planning, and advisory boards Serves as the medical representative within Product Development sub-teams (including Clinical, V&I, Commercial, Publications, and ... Job Description Role Summary: The Global Senior Director Medical Affairs (GDMA) is a subject matter...symposia and educational meetings. Supports key countries with the development of local data generation study concepts and protocols… more
- Merck & Co. (Rahway, NJ)
- …of progressive experience in HF within pharmaceutical, medical device, or combination product development .Proven track record of leading and growing HF teams ... Development & Technology (DD&T) engaged across the entire product lifecycle-from early development through commercialization and post-market… more
- Merck & Co. (Rahway, NJ)
- …to the Regulatory Affairs, R&D, Manufacturing and GHH management teams, product development teams, and executive management.Establishes strong cross-functional ... expertise in CMC regulatory strategy and dossier management activities across product development , registration, and life-cycle management.A strong track record… more
- Merck & Co. (Rahway, NJ)
- …activities/projects - Willingness to grow and learn all areas of Pharmaceutical new product development - - Preferred Experience and Skills: - Medical Device ... Director , Engineering, Packaging Commercialization will lead packaging development for new products including parenteral products including small molecules,… more
- Merck & Co. (Rahway, NJ)
- …Decision Making, Deviation Investigations, Driving Continuous Improvement, Drug Product Development , Estimation and Planning, Fast-Paced Environments, ... Good Manufacturing Practices (GMP) facility within the Process Research and Development (PR&D) organization which enables gain of critical internal experience during… more
- Merck & Co. (Rahway, NJ)
- …including packaging commercialization, quality, analytical, regulatory, manufacturing, Device Development and Technology, Technical Product Leaders, and ... Job DescriptionDir, Engineering - Director , Assembly and Packaging Platform Technical LeadershipReporting into...ensuring the successful completion of projects. This includes the development and execution of robust technical plans across device… more
- Formation Bio (New York, NY)
- …strategic and tactical plans. Identifies and assesses regulatory risks associated with product development for Formation Bio's drug assets. Represents the ... and AI driven pharma company differentiated by radically more efficient drug development . Advancements in AI and drug discovery are creating more candidate drugs… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …as we work together to change lives for the better. The Position The Director , Media Relations & Issues Management is accountable for establishing and leading Novo ... to dramatically influence stakeholder perceptions. Relationships Reports to the Senior Director , Media & Stakeholder Relations, and interacts with senior leaders… more
- Taiho Oncology (New York, NY)
- …evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower ... team at Taiho Oncology Inc. As a Regional Business Director (RBD), you will play a crucial role in...will be instrumental in promoting Taiho Oncology Inc's approved product line to our external customers, ensuring high visibility… more
- MetroPlusHealth (New York, NY)
- …committed to building strong relationships with its members and providers.Position OverviewThe Director of State Product Compliance, reporting to the Vice ... plays an integral role in the oversight and management of product regulatory compliance activities, for State products offered by MetroPlusHealth including… more
