- Merck & Co. (Rahway, NJ)
- …Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage ... clinical trials (design, operational plans, settings) based on these clinical development strategiesMonitoring and managing the conduct of ongoing or… more
- Novo Nordisk Inc. (Boulder, CO)
- About the Department Our Research & Development organization brings together the best minds in life science innovation. The teams located in facilities in Lexington, ... Seattle reflect the full R&D continuum, from early research through late-stage clinical development . Here, we are building for the future, creating a distinct R&D… more
- Repligen (Waltham, MA)
- …and driven IT Business Partner to represent our Manufacturing, Quality, Supply Chain, Product Development , and R&D organizations. As a Director of IT, you will ... and enabling innovation across the bioprocessing manufacturing and product development lifecycle.This position requires strong collaboration with business leaders… more
- Eisai, Inc (Philadelphia, PA)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... If this is your profile, we want to hear from you. The Associate Director of Global Submission Management (GSM) is responsible for leading, managing ,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …program(s). Provides managerial oversight to colleagues that they are directly line managing in their group. They will ensure their direct reports are meeting ... and putting appropriate measures in place to course correct where needed. The Director will be accountable to support SDL and employee personal development ,… more
- Merck & Co. (Rahway, NJ)
- Job Description Associate Director , Regulatory Submissions Archive Operations - Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) - Functional ... Regulatory Affairs & Clinical Safety (GRACS) - The Associate Director of Regulatory Submissions Archive Operations serves as the...Veeva RIM Submissions Archive and is also responsible for managing the physical paper archives for GRACS. This dual… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Associate Director Global Medical Affairs Oncology (GMA), under the direction of the ... Senior Director / Director , GMA Oncology (Global Medical Affairs team...within a specific compound or indication.Responsibilities- Support GMA the development of the Global Medical Affairs strategy and execution… more
- Insmed Incorporated (NJ)
- …global regulatory strategies and plans to enable efficient, competitive product development for assigned programs. This role will provide regulatory input to ... global cross-functional project teams throughout product development and submission activities. The GRL will serve as the global regulatory lead for documentation… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …together to change lives for the better. The Position The Associate Director , Consumer Social Media Strategy is a high-impact, hands-on leadership role responsible ... for the development , execution and optimization of all consumer-facing content and...translates the corporate digital vision set by the Senior Director into best-in-class digital experiences, driving audience engagement, building… more
- Eisai, Inc (Nutley, NJ)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... your profile, we want to hear from you. The Director , Global Regulatory, Growth Markets will be responsible for...in growth markets. This role will focus on the development and execution of regulatory strategies for products under… more
