• Research Associate II

    WuXi AppTec (San Diego, CA)
    …is expanding its in vivo Pharmacology Division. We're seeking a highly motivated Research Associate II to join the team. **Responsibilities** * Assisting and ... assay development, optimization, and validation projects * Following SOPs to perform compound receiving, registration, and management * Help to manage lab… more
    WuXi AppTec (01/17/25)
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  • Associate Scientist II, Animal Care…

    J&J Family of Companies (Spring House, PA)
    Johnson & Johnson is recruiting for Associate Scientist II, Animal Care & Research Support to join our team in Spring House, PA. At Johnson & Johnson, we believe ... responsibility of the Associate Scientist II is to provide in vivo research support, animal care and scientific collaboration. The Associate Scientist II is… more
    J&J Family of Companies (01/31/25)
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  • Scientific Business Analyst ( Research

    Amgen (South San Francisco, CA)
    …tools for drug design, Electronic Lab Notebooks (ELN), Laboratory Information Management Systems (LIMS), and compound registration systems. + **Cheminformatics ... chemistry data, experimental results, and external databases, ensuring efficient data management and accessibility across research teams. + **Data… more
    Amgen (01/12/25)
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  • Associate Medical Director, Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …relationship between Takeda and partner. ​ ​Leadership, Task Force Participation, Upper Management Accountability + Interacts with research division and other ... will inspire you and empower you to shine? Join us as an Associate Medical Director, Clinical Science in our Gastrointestinal & Inflammation Therapeutic Area Unit--… more
    Takeda Pharmaceuticals (02/07/25)
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  • Associate Medical Director, Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …relationship between Takeda and partner. ​ ​Leadership, Task Force Participation, Upper Management Accountability + Interacts with research division and other ... that will inspire you and empower you to shine? Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge, MA office.… more
    Takeda Pharmaceuticals (01/31/25)
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  • Associate Director, Clinical Supply Project…

    Merck (Rahway, NJ)
    …process & connectivity between functions supporting pipeline (ie clinical development, Compound Management Coordination , supply chain, & human health), ... packaging activities as well as supply chain documentation to support critical Compound Management Coordination activities. + Support the collection of clinical… more
    Merck (01/16/25)
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  • Associate Vice President/Therapeutic Area…

    Merck (West Point, PA)
    …support of the Common Technical Document (CTD) and label, including relevant compound /program life-cycle management . The successful candidate will have an ... **Job Description** The Associate Vice President (AVP) will be responsible for...experience with the principles of drug development to ensure compound transition along the pipeline, management experience,… more
    Merck (01/22/25)
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  • Associate Director, Biostatistics…

    Gilead Sciences, Inc. (Foster City, CA)
    …operational statistical activities for a group of clinical trials for a compound /indication or equivalent through management of internal and external resources ... and help create possible, together. **Job Description** Job Description ** Associate Director, Biostatistics** **Position Overview:** Are you passionate about… more
    Gilead Sciences, Inc. (12/05/24)
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  • Sr. Research Investigator , Clinical…

    Bristol Myers Squibb (Princeton, NJ)
    …scientific principals and data. **Responsibilities** + **Independently contribute** to compound development across various development phases + **Represent** Clin ... + Advanced Degree in related field (MS, Ph.D. or PharmD) + For Associate Director level with Ph.D. approximately 5+ years experience with demonstrated progression… more
    Bristol Myers Squibb (02/07/25)
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  • Associate Director, Safety Data Architect…

    AbbVie (Springfield, MA)
    …biomedical disciplines). Graduate degree preferred. 10 years of experience in clinical research in the pharmaceutical industry. + Project management experience ... drives consistency across clinical trial protocols through contribution to the safety management plan. Responsibilities: + Functions as a driver for data in… more
    AbbVie (02/05/25)
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