• Associate Director, Alliance Vendor…

    Teva Pharmaceuticals (West Chester, PA)
    Associate Director, Alliance Vendor Relationship Manager Date: Jul 22, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals ... and new people to make a difference with. **The opportunity** The Associate Director, Alliance/Vendor Relationship Manager will be responsible for managing and… more
    Teva Pharmaceuticals (07/23/25)
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  • Associate /Sr. Associate - QA…

    Lilly (Indianapolis, IN)
    …to make life better for people around the world. **Organization Overview:** The Associate - QA provides quality oversight of the distribution of Clinical Trial ... to ensure quality and timely delivery of CT material to patients. The Associate - QA provides quality oversight of the Temperature Excursion Investigation Center… more
    Lilly (07/09/25)
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  • Senior Associate Paralegal, Patent…

    Amgen (Thousand Oaks, CA)
    …us and transform the lives of patients while transforming your career. Senior Associate Paralegal, Patent Litigation **What you will do** Let's do this. Let's change ... of discovery (including witness interviewing and electronic and paper document collection), trial preparation, trial support and case management as a member… more
    Amgen (06/12/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills and… more
    Merck (07/26/25)
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  • CRA III ( Associate Clinical Research III)

    Abbott (Alameda, CA)
    …new study investigators and writing and assembling submissions. + Maintain and audit Trial Master File to ensure inspection readiness. + Perform review of clinical ... required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and Reports). +...+ Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data… more
    Abbott (06/27/25)
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  • Associate Vice President Cardiometabolic…

    Lilly (Indianapolis, IN)
    …in metabolic dysfunction-associated steatohepatitis (MASH) trials, to support a future MASH outcome trial . - The CRP will work with a broader team of physicians on ... the day-to-day medical operations of the trial and will report to the AVP/Medical Director- Incretin...critical role in the daily medical leadership of the trial , while also playing an executive and mentoring role.… more
    Lilly (06/27/25)
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  • Open Rank- Assistant Professor/ Associate…

    University of Colorado (Aurora, CO)
    **Open Rank- Assistant Professor/ Associate Professor** **Description** **University of Colorado Anschutz Medical Campus** **Department: Pediatrics - ... Hematology/Oncology** **Job Title:** **Open Rank- Assistant Professor/ Associate Professor** **Position #: 00008181 - Requisition #:36015** **Job Summary:** Key… more
    University of Colorado (07/30/25)
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  • Associate

    Robert Half Legal (Walnut Creek, CA)
    …and organized manner * Conduct depositions, preparing witnesses for deposition and trial * Review and analyze discovery requests, preparing and responding to ... accounted for * Utilize your skills in defending depositions, trial experience, and civil litigation to effectively carry out...Candidate must have experience in the role of an Associate . * Demonstrated ability to defend depositions effectively. *… more
    Robert Half Legal (07/29/25)
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  • Associate Scientific Director,…

    AbbVie (Mettawa, IL)
    …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director provides medical and scientific strategic and operational input ... + Participates in the design and execution of clinical trial safety, product safety and risk management plans. May...strongly preferred. + Minimum of 5 years of clinical trial or medical affairs experience in the pharmaceutical industry.… more
    AbbVie (07/26/25)
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  • Associate Director, Clinical and Safety…

    Takeda Pharmaceuticals (Boston, MA)
    …to the best of my knowledge. **Job Description** **About the role:** The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the ... considered. + Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects. Actively participate and… more
    Takeda Pharmaceuticals (07/25/25)
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