• Director, Analytical R&D

    Merck (Rahway, NJ)
    …Analytical Technology (PAT), Professional Networking, Regulatory Compliance, Regulatory Submissions, Results-Oriented, Talent Development , Team Leadership, ... DSCS teams. This role has a wide responsibility for analytical method development and testing for chemical and biocatalytic synthetic processes, and / or… more
    Merck (08/08/25)
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  • Senior Principal Scientist, Upstream Process R&D

    Merck (Rahway, NJ)
    …scientific leader with expertise in downstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Senior Principal Scientist. BPR&D ... within Research Laboratories is committed to rapidly delivering diverse biotherapeutics...upstream processes for biologics in various stages of clinical development , as well as process characterization and regulatory more
    Merck (07/24/25)
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  • Library Senior Specialist, Knowledge Management

    Merck (Rahway, NJ)
    …Description** Be part of a dynamic team that is dedicated to accelerating research and innovation. We are seeking a passionate and knowledgeable Senior Specialist to ... you will be playing a pivotal role in advancing research by linking our stakeholders with scientific and medical...team members on user acceptance testing and to system development lifecycle **Education** + Degree in life sciences, information… more
    Merck (07/31/25)
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  • Vice President, US Medical Affairs & Global…

    Teva Pharmaceuticals (Parsippany, NJ)
    …The ideal candidate will have extensive experience in medical affairs, clinical development , and a proven track record of successful leadership in the pharmaceutical ... will have, strong leadership, a deep understanding of medical affairs, clinical development in the pharmaceutical or biotechnology industry, and the ability to drive… more
    Teva Pharmaceuticals (06/20/25)
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  • Director, Pharmacometrics (Remote or Hybrid)

    Merck (Rahway, NJ)
    …discovery and development (MIDD) to routinely enable efficient drug discovery/ development and/or regulatory decisions. The Pharmacometrics group within QP2 ... in pharmacometrics with ability to understand how MIDD can drive portfolio and regulatory decisions + Deep knowledge of drug development , pharmacokinetics and… more
    Merck (08/08/25)
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  • Senior Medical Science Liaison - Biopharma…

    Sumitomo Pharma (Jersey City, NJ)
    …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... as well as provide education of priority customers on research and development projects. + Accumulate key...+ Advanced degree in medical science (MD, PharmD, or PhD ) is strongly preferred. Candidates without an advanced degree… more
    Sumitomo Pharma (07/23/25)
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  • Sr Manager, Supply Chain

    Gilead Sciences, Inc. (Parsippany, NJ)
    …with Clinical Operations, Formulation Process Development , Device Development and Clinical Package Engineering, Quality Assurance, Regulatory , ... member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we… more
    Gilead Sciences, Inc. (07/22/25)
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  • Director, Medical Affairs Strategy (Prostate…

    Sumitomo Pharma (Trenton, NJ)
    …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... field forces to work together. + Partner with the Research & Development organization for ongoing and...field required. + Advanced degree in medical science (MD, PhD ); MD with relevant specialization preferred. + 8+ years… more
    Sumitomo Pharma (07/30/25)
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  • Director, Neurology and Immunology HEVA Business…

    Sanofi Group (Morristown, NJ)
    … in the forms of economic modelling, database analysis, observational research , Clinical Outcomes Assessment (COA) development and validation, systematic ... global development team that is responsible for designing clinical research programs to meet the evidentiary standards of regulators, HTA organizations,… more
    Sanofi Group (05/26/25)
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  • Sr. Study Manager - Oncology

    Merck (Rahway, NJ)
    …any study specific partners and/or vendors. **Core Skills:** + Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH) + Ability to manage ... drug development , project management, and/or medical field experience or PhD /PharmD Degree Degree in life sciences, preferred. -15% Travel Current Employees… more
    Merck (08/08/25)
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