• Director, Analytical R&D

    Merck (Rahway, NJ)
    …candidate will establish a viable succession plan for key positions within SMAR&D ( scientific and management pathways), including their own role. The position is ... is expected, as is as advancing a culture of scientific excellence, GMP and compliance mindset, and collaboration with...Duties & Responsibilities include: + Analytical methodologies + Project management skills + Review and approval of data more
    Merck (08/08/25)
    - Related Jobs
  • Sr Technologist

    Mondelez International (East Hanover, NJ)
    …screen panelists, manage panel performance, and enforce lab rules to ensure reliable data collection + Support and occasionally lead roundtable discussions and ... assigned projects or offer functional services. Using your fundamental understanding of data collection, you will assess for compliance and take corrective measures… more
    Mondelez International (08/28/25)
    - Related Jobs
  • Associate Director, Global Regulatory Affairs…

    Sanofi Group (Morristown, NJ)
    …strategy for assigned products, including those in clinical development, life cycle management (LCM), and the marketed portfolio. This role leads the creation and ... update of core labeling documents (eg, Company Core Data Sheet) and regional labeling (eg, US Prescribing Information, EU SmPC), ensuring alignment with regulatory… more
    Sanofi Group (06/27/25)
    - Related Jobs
  • Director, Global Health Economics, Value,…

    Teva Pharmaceuticals (Parsippany, NJ)
    …GHEVO deliverables in preparation for asset launches. ⦁ Represent Teva externally at scientific , medical, regulatory, and payer meetings. ⦁ Stay abreast of trends in ... a network of clinical, GHEVO, and payer experts to support market access strategies. ⦁ Manage project budgets and...⦁ Manage project budgets and timelines. ⦁ Contribute to scientific communications and publications. ⦁ Ensure all initiatives remain… more
    Teva Pharmaceuticals (08/08/25)
    - Related Jobs
  • Clinical Development Program Lead, Neuropsychiatry…

    Bristol Myers Squibb (Madison, NJ)
    …clinical trial, drug development, and regulatory experience, in addition to a strong scientific background + Management experience will be important since this ... with teams in R & ED and GDD to support GT4/5 and POC transitions, providing insights into biology,...develop programs beyond commercialization and launch and into lifecycle management Leadership and Matrix Management + Lead… more
    Bristol Myers Squibb (08/30/25)
    - Related Jobs
  • Detailed Scheduling Global Process Steward

    Sanofi Group (Morristown, NJ)
    …like Planning, Purchasing, Procurement, Production, Warehousing, Distribution, Quality and Master Data . The Steward will also support their domains System ... (eg Global and Site Data Stewards, Key Users, etc. for Warehousing) + Support for global harmonization of the domains specific master data and business… more
    Sanofi Group (06/27/25)
    - Related Jobs
  • Regulatory Strategist

    Sanofi Group (Morristown, NJ)
    …activities, including generating submission content plans, submission tracking, and document management utilizing the support and input of cross-functional team ... for products in development as well as for lifecycle management of products. + May serve as a regional/local...of the briefing document focused on the strategy and scientific content, leading the team through meeting preparations and… more
    Sanofi Group (07/30/25)
    - Related Jobs
  • Director, Taip TA Lead - Trial Analytics, Insights…

    Bristol Myers Squibb (Princeton, NJ)
    …and site prioritization approaches + Champion use of platforms, tools, and data infrastructure that support delivery excellence + Integrate analytics with ... measurement, mitigation and management , including timely issue review, escalation and management to support trend analysis and risk prevention. If you come… more
    Bristol Myers Squibb (08/30/25)
    - Related Jobs
  • Director, Clinical Operations

    Bausch + Lomb (Trenton, NJ)
    …site monitoring), scientific methods, research design, regulatory compliance, and clinical data management . + Minimum 10-12 years experience in the industry ... etc. + Liaise with PVG/GPSS and provide clinical operations support and guidance for the ongoing surveillance of the...of the events to the IRBs/REBs/ECs. + Liaise with Data Management to review data more
    Bausch + Lomb (06/07/25)
    - Related Jobs
  • Senior Staff/Senior DevOps Engineer

    SciTec (Princeton, NJ)
    …the mission to deliver advanced sensor data processing technologies and scientific instrumentation capabilities in support of National Security and Defense. ... Government in building innovative new tools to deliver unique world-class data exploitation capabilities. Important Notice: SciTec exclusively works on US government… more
    SciTec (08/10/25)
    - Related Jobs