• Daiichi Sankyo, Inc. (Bernards, NJ)
    …authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will collaborate ... stakeholders. Collaboration with external stakeholders (eg, research pharmacists, clinical study partner management) may also be required. Additionally, the… more
    HireLifeScience (05/18/25)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director , has primary responsibility for ... and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case… more
    HireLifeScience (05/30/25)
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  • Merck & Co. (San Francisco, CA)
    …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
    HireLifeScience (05/29/25)
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  • Merck & Co. (Boston, MA)
    Job DescriptionWe are seeking a highly skilled and motivated Associate Principal Scientist/ Associate Director with expertise in conducting outcome ... real world data is preferred.Experience with outcomes research, including RWE studies , throughout the product lifecycle within biomedical research and/or healthcare… more
    HireLifeScience (05/30/25)
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  • Merck & Co. (Rahway, NJ)
    …plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have demonstrated ... and ensures proper allocation of drug product as needed across studies within assigned program(s).-Responsible for identifying significant supply risks associated… more
    HireLifeScience (05/29/25)
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  • Merck & Co. (Rahway, NJ)
    … will manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate… more
    HireLifeScience (05/24/25)
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  • Genmab (NJ)
    …and development of data-driven early indication and program assessments, study -level feasibility assessments, robust country and site identification, ... and processes to inform risk-benefit decision making at TA, program and study levels.This position reports to our Princeton, NJ office and is… more
    HireLifeScience (05/16/25)
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  • Eisai, Inc (Nutley, NJ)
    …May provide training on GCP and current regulations for those undertaking clinical studies .Job SummaryThe Associate Director , GCP Quality Assurance works ... (approximately 25%)Eisai Salary Transparency Language:The base salary range for the Associate Director , Clinical Quality Assurance is from :159,500-209,400Under… more
    HireLifeScience (05/07/25)
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  • Merck & Co. (Rahway, NJ)
    …West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology ... pipelines. - As an Associate Director , you will represent QP2 on...with external vendors and partners, on activities related to study design, protocol development, study execution, reporting… more
    HireLifeScience (05/03/25)
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  • Merck & Co. (Boston, MA)
    Job DescriptionThe Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities involving ... Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. The Executive Director will manage and oversee the entire cycle of late stage clinical… more
    HireLifeScience (05/24/25)
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  • Merck & Co. (Millsboro, DE)
    …within the Global Safety & Environment organization, and reports to the Associate Director of Safety & Environment at Millsboro, DE.Responsibilities:Ensure ... effective Biosafety program at the Millsboro, Delaware Animal Health site . The successful candidate will play a key role...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
    HireLifeScience (05/17/25)
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  • Associate Director , Study

    Takeda Pharmaceuticals (Boston, MA)
    …innovation-driven company to inspire you and empower you to shine? Join us as an Associate Director , Study Site Engagement based remotely reporting to ... contributor to our inspiring, bold mission. **_GOALS:_** + The Associate Director , Study Site...and provides updates on planned and ongoing global clinical studies , with a focus on country landscaping, upcoming feasibilities,… more
    Takeda Pharmaceuticals (05/30/25)
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  • Associate Director , Program Lead…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will collaborate ... stakeholders. Collaboration with external stakeholders (eg, research pharmacists, clinical study partner management) may also be required. Additionally, the… more
    Daiichi Sankyo Inc. (05/08/25)
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  • Associate Director - QA Batch…

    Lilly (Durham, NC)
    …ongoing operation as well as site inspection readiness and execution. The Associate Director reports to the Site Quality Leader. **Key ... around the world. **Position Description** : The Quality Assurance Associate Director is responsible for support of...materials, semi-finished and finished goods for the RTP production site . The role will help build a strong quality… more
    Lilly (05/01/25)
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  • Associate Director , Translational…

    J&J Family of Companies (Spring House, PA)
    …every step of the way. Johnson & Johnson is recruiting for an Associate Director , Study Responsible Physician (SRP) Immunology Translational Sciences ... MA, San Diego, CA. The primary focus of this Associate Director , Study Responsible Physician...collaboration with other functions in GDO: + Participates in study feasibility, CRO/ site selection, trial preparation, initiation,… more
    J&J Family of Companies (05/30/25)
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  • Associate Director of Native…

    Stanford University (Stanford, CA)
    Associate Director of Native American Studies **School of Humanities and Sciences, Stanford, California, United States** Administration Post Date Dec 20, ... an undergraduate program within the Center for the Comparative Study of Race and Ethnicity (CCSRE) within the School...**Native American Studies Program is seeking an Associate Director . The Associate more
    Stanford University (04/24/25)
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  • Director , Los Angeles Programs,…

    Boston University (Boston, MA)
    …faculty and staff at Boston University (all course proposals are reviewed by the BU Study Abroad Associate Director of Academic Affairs and approved by the ... BU policies and training opportunities. **Academics [25%]** + Oversee site curriculum of LA Programs, working closely with BU...Executive Director and the Associate Director of Academic Affairs, BU Study Abroad,… more
    Boston University (05/02/25)
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  • Associate Director , Feasibility

    Takeda Pharmaceuticals (Boston, MA)
    …company to inspire you and empower you to shine? Join us as an Associate Director , Feasibility based remotely reporting to the Director , Feasibility. ... Conduct data-driven feasibility assessments for Phase I - IV clinical studies , including protocol design optimization, country/ site identification, enrollment… more
    Takeda Pharmaceuticals (05/30/25)
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  • Study Coordinator I

    Charles River Laboratories (Ashland, OH)
    …(as needed). + Ability to compile and/or interpret scientific data, meeting with Study Director /Pl as needed. + Provide editorial/formatting review of final ... study progress (as applicable) and generation of end-of- study reports for assigned studies with a...text (as applicable). Provide comments and/or suggested changes to Study Director /Pl. + Proficient in generating reports… more
    Charles River Laboratories (05/20/25)
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  • Research Associate - Center for Puerto…

    CUNY (New York, NY)
    Research Associate - Center for Puerto Rican Studies (Multiple Positions) **GENERAL DUTIES** Conducts academic research in connection with CUNY programs; may ... by the University and relevant outside parties **CONTRACT TITLE** Research Associate **FLSA** Exempt **CAMPUS SPECIFIC INFORMATION** The Center for Puerto Rican… more
    CUNY (05/01/25)
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