• Merck & Co. (Boston, MA)
    …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. (Boston, MA)
    … 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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  • 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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  • 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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  • 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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  • Senior Study Manager

    Actalent (Boston, MA)
    …address issues, and provide expert-level guidance. The position reports to an Associate Director and involves both strategic planning and operational execution ... clinical studies . Responsibilities + Lead the development of clinical study plans, identifying critical path activities and interdependencies. + Create and… more
    Actalent (05/29/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …application is true to the best of my knowledge. **Job Description** ** Associate Director , Clinical Research, Value & Evidence Generation, US Medical** ... of all US Medical Clinical Research including, Medical Affairs Company Sponsored Studies (MACS) collaborative studies and Investigator Initiated Research (IIR).… more
    Takeda Pharmaceuticals (05/03/25)
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  • Associate Director , Quantitative…

    Merck (Cambridge, MA)
    …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
    Merck (05/03/25)
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  • Senior Manager - Associate Director

    Sumitomo Pharma (Boston, MA)
    …Overview** We are currently seeking a versatile and experienced Senior Manager - Associate Director level scientist with strengths in clinical pharmacology, and ... drug metabolism and bioanalytic chemistry. This position will report to Senior Director of Clinical Pharmacology and Drug Metabolism. S/he will work across… more
    Sumitomo Pharma (05/14/25)
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  • Associate Medical Director

    Sumitomo Pharma (Boston, MA)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... a medical safety subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study more
    Sumitomo Pharma (05/16/25)
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  • Associate Director , Oncology…

    Bristol Myers Squibb (Cambridge, MA)
    …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director and Group Leader, Oncology Discovery Biology The Oncology ... centers in the area. Our Bristol Myers Squibb research site in Cambridge Crossing will help us continue to...innovation, and business opportunities. **Position Summary** The role of Associate Director , Oncology Discovery Biology within the… more
    Bristol Myers Squibb (05/29/25)
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  • Associate Director , Quantitative…

    Merck (Boston, MA)
    …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
    Merck (05/30/25)
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  • Senior Director , Clinical Research,…

    Merck (Boston, MA)
    … will manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... drugs + Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as...to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring… more
    Merck (05/24/25)
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  • Associate Principal Scientist/…

    Merck (Boston, MA)
    **Job Description** We are seeking a highly skilled and motivated Associate Principal Scientist/ Associate Director with expertise in conducting outcome ... data is preferred. + Experience with outcomes research, including RWE studies , throughout the product lifecycle within biomedical research and/or healthcare… more
    Merck (05/30/25)
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  • Associate Director / Director

    Bristol Myers Squibb (Cambridge, MA)
    …of BMS current and future therapeutics. **Summary** Reporting to Executive Director , Translational Development, the incumbent will be part of the translational ... the preclinical support of asset programs through mechanism of action-based studies , differentiation from standard of care molecules, combination rationale and… more
    Bristol Myers Squibb (05/27/25)
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  • Executive Director , Product Development…

    Merck (Boston, MA)
    **Job Description** The Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities ... Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. The Executive Director will manage and oversee the entire cycle of late stage clinical… more
    Merck (05/24/25)
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  • Associate Director , Strategic…

    Takeda Pharmaceuticals (Boston, MA)
    …excellence and portfolio progression for the Takeda Research pipeline. The AD/ Director of Strategic Outsourcing will provide strategic oversight and relationship ... that foster mutual growth and learning. + Conduct CRO site qualification visits and select CROs based not only...understanding of FDA Good Laboratory Practices (GLP) for nonclinical studies as set forth in 21 CFR Part 58,… more
    Takeda Pharmaceuticals (05/04/25)
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  • Medical Director

    Grifols Shared Services North America, Inc (Boston, MA)
    …in more than 110 countries and regions. **Position Overview:** The Medical Director will be responsible for clinical strategy relating to upcoming clinical trials, ... are not limited to the following:** + Design of trials, including study population and eligibility criteria, treatment duration, clinical endpoints, biomarkers, and… more
    Grifols Shared Services North America, Inc (05/30/25)
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