- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The GCO Senior Director of Study Optimization has accountability for the oversight, ... and external stakeholders and ensure successful delivery of the clinical studies.Responsibilities:Guide strategy and delivery of GCO...in role such as a Global Project Leader at Sr . Director level or equivalent requiredRelevant therapeutic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. Summary: The position will define and oversee the translational medicine strategy for a drug program across multiple indications. The successful candidate ... will set goals and enumerate key scientific questions that will drive clinical development decision-making. In doing so, he or she will align closely with the Global… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director , USMA Oncology (US Medical Affairs team lead for compound), is ... and resources for the assigned medical affairs plan activities, in collaboration with Sr . Director .- Leads medical readiness activities for market launches. This… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …leader for assigned compound under the supervision and leadership of the Executive Director of Medical Research and Strategy , US Oncology Medical Affairs ... (USOMA). Develops the USOMA strategy and tactical plan as part of the US...member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Job Summary: Director , Global QA Strategy &Operations (Global R&D PV QA) is responsible ... R&D PV QA and the Head of Global QA Strategy and Operations to ensure alignment and execution of...high impact.Ability to effectively interact with and present to senior management at all levels, as well as to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …all Medical Affairs programs. This role involves deputizing for the Sr . Director , representing the Quality organization at senior levels. The Director ... compliance and working toward building a quality mindset with Medical Affairs.Support the Sr . Director 's Medical Affairs Quality strategy by partnering with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …leadership of the Global Medical Affairs (GMA) Franchise Head. Develops the GMA early strategy and tactical plan and leads the execution of the activities in the GMA ... plan.Responsibilities- Responsible for the development of the Global Medical Affairs early strategy and medical objectives for the portfolio of early asset compounds… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. Summary:The primary responsibilities of this position are to guide the strategy and to lead the implementation of companion diagnostics (CDx) in support ... drug registration or for any project with CDPs containing multiple registrational clinical trials and are extensively exploring the predictive nature of potential… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Director Global Medical Affairs Oncology (GMA), under the direction of the Senior Director / Director , GMA Oncology (Global Medical Affairs team lead for ... for the assigned GMA plan activities, in collaboration with Sr Director .- Support medical readiness activities for...and other scientific exchange activities in alignment with the Senior Director , such as scientific symposium and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the potential to dramatically influence stakeholder perceptions. Relationships Reports to the Senior Director , Media & Stakeholder Relations, and interacts with ... 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… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director ( Sr . Principal Scientist) has primary responsibility for the planning and directing clinical research activities ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director...Director will manage the entire cycle of late-stage clinical development and studies, including development strategy ,… more
- Merck & Co. (Rahway, NJ)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... further study of marketed compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical Scientists in the execution of… more
- Merck & Co. (Rahway, NJ)
- Job Description Role Summary: The Global Senior Director Medical Affairs (GDMA) is a subject matter expert in their area of responsibility (eg, defined tumor, ... and tactical execution. Communicates pertinent information to stakeholders (eg, Executive Director Medical Affairs (EDMA), Regional Strategy Leads (RSL),… more
- Merck & Co. (Rahway, NJ)
- …to enhance patient safety and product usability. The Senior Director will champion enterprise-wide HF strategy , foster cross-functional collaboration, and ... Job DescriptionThe Senior Director of Human Factors (HF)...to the HF team and key stakeholders across R&D, clinical , regulatory, marketing, manufacturing, and quality functions.Educate and build… more
- Merck & Co. (Rahway, NJ)
- …and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal ... strategies for assigned drug-device combination product program(s) for successful clinical introduction(s) and commercial market(s) approval(s).Define design input(s)/ output(s)… more
- Merck & Co. (Rahway, NJ)
- …modality or traditional solid-oral small molecules and includes pre-approval regulatory strategy and submissions (global clinical and marketing applications such ... and dedicated colleagues while developing and expanding your career.The Executive Director , Chemistry, Manufacturing & Controls ( CMC) , Pre-approval Pharm will… more
- Merck & Co. (Rahway, NJ)
- …and Commercial. Understanding of product development lifecycle and integration of CMC and clinical strategy and ability to engage to ensure product is positioned ... organization for our company's Manufacturing Division product supply chain strategy in alignment with Global Human Health brand/franchise commercial goals.… more
- Eisai, Inc (Nutley, NJ)
- …mgmt. activities. #LI-CCEisai Salary Transparency Language:The base salary range for the Senior Director , Clinical Quality Assurance - Remote-Based is ... position is responsible for design, delivery and execution of the global Clinical Quality Assurance (CQA) strategy including audit and inspection management,… more
- Formation Bio (New York, NY)
- …proof-of-concept models into scalable, production-ready systems Define technical execution strategy for clinical outcome prediction, indication expansion, and ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
