• Associate Director - Clinical

    Lilly (Branchburg, NJ)
    …life better for people around the world. **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational ... to improve performance and speed drug development. **Responsibilities:** + Deliver improved clinical trial supply chain performance, assess and mitigate risk,… more
    Lilly (09/20/24)
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  • Senior Manager, Clinical Trial

    AbbVie (New York, NY)
    clinical trial populations. This role will report into the Associate Director , Diversity & Patient Inclusion. Responsobilties: + Drive the strategic ... required by the FDA for all clinical studies (PhIII) to improve clinical trial diversity. With this role, you will be an important member of the team… more
    AbbVie (09/20/24)
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  • Associate Director , Clinical

    AbbVie (Branchburg, NJ)
    …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Development will have global or ... Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director ,...responsible for: + Ensuring alignment between the IEST, and Clinical Trial Team(s) + Developing the proposed… more
    AbbVie (09/20/24)
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  • Associate Director , Clinical

    Bristol Myers Squibb (Berkeley Heights, NJ)
    …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Clinical Data Standards is a leadership role ... This role reports to Director or Executive Director , Head Standards Management & Steward within Clinical...and optimal approaches to support the end to end clinical trial data lifecycle, from collection through… more
    Bristol Myers Squibb (09/21/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors… more
    Regeneron Pharmaceuticals (07/04/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... + Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates management… more
    Daiichi Sankyo Inc. (07/21/24)
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  • Associate Director , Clinical

    Gilead Sciences, Inc. (Parsippany, NJ)
    …specializes in process improvements, procedural documents, and quality and inspection readiness for Clinical Operations. The Associate Director , will be a ... Join Gilead and help create possible, together. **Job Description** The Clinical Trial Capabilities (CTC) organization offers infrastructure, support, and… more
    Gilead Sciences, Inc. (09/21/24)
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  • Clinical Research Associate I Safety…

    Mount Sinai Health System (New York, NY)
    …safety aspects of clinical research trial (s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible for ... clinical studies as a clinical trial assistant or clinical research associate...for adjudication by the CEC. + Participates with the Associate Director of Research and Quality Outcomes… more
    Mount Sinai Health System (08/02/24)
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  • Associate Director , Informed…

    Bristol Myers Squibb (Madison, NJ)
    …This includes a centralized triage function for informed consent negotiations with global clinical trial sites, IRBs/ECs, and health authorities, as well as ... internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role...Simplification. + Knowledge of IT systems used to support clinical trial processes and the authoring of… more
    Bristol Myers Squibb (09/21/24)
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  • Medical Director Oncology Clinical

    AbbVie (Florham Park, NJ)
    …Completion of a subspecialty fellowship is desirable. + At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. + ... to support a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical more
    AbbVie (09/20/24)
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  • Associate Director , Medical Affairs…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Associate Director , Medical Affairs, Movement Disorder/Parkinson's Disease will be ... (ND0612) and related diseases in close collaboration with cross-functional colleagues. The Associate Director , Medical Affairs will serve as a subject matter… more
    Mitsubishi Chemical Group (07/19/24)
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  • Associate Director , External…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …other research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director will lead the execution and lifecycle management of ... Research (CESR) projects. Candidates should have a comprehensive understanding of clinical trial management, with firsthand experience managing collaborative… more
    Daiichi Sankyo Inc. (07/27/24)
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  • Associate Director , Biostatistics

    Bristol Myers Squibb (Berkeley Heights, NJ)
    …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning,… more
    Bristol Myers Squibb (08/25/24)
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  • Associate Director , PED Policy…

    AbbVie (Newark, NJ)
    …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Patient Experience Data (PED) Policy & Best Practices, ... areas for AbbVie in alignment with external policy and scientific advancements. The Associate Director , PED Policy & Best Practices, will cultivate strong… more
    AbbVie (09/20/24)
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  • Associate Director ; Advanced…

    Merck (Rahway, NJ)
    …mission to achieve new milestones in global healthcare. Our company's Global Clinical Trial Operations (GCTO) organization is primarily responsible for executing ... late-stage clinical trials across therapeutic areas around the globe. The Associate Director , Advanced Analytics will work with our partners across GCTO to… more
    Merck (09/27/24)
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  • Associate Director , Biostatistics

    Pfizer (New York, NY)
    …communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results **,** ... biostatistics, or related field. + A minimum of 4 years' experience in the clinical trial setting (preferably in oncology of Pharma). + Relevant clinical more
    Pfizer (09/06/24)
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  • Associate Director , North America…

    Bristol Myers Squibb (Summit, NJ)
    …and the ability to help patients are incredible. **The Position:** The Associate Director , North America Operations and Global Process Support, Scheduling ... and commercial Cell Therapies in North America. The Associate Director , North America Operations and Global...in global, highly matrixed teams to support launch readiness, clinical trial readiness, life cycle management, and… more
    Bristol Myers Squibb (09/30/24)
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  • Translational Medicine Sr. Principal Scientist/…

    Bristol Myers Squibb (Summit, NJ)
    …stage drug development + Experience in activities required for and related to clinical trial initiation, maintenance and completion + Experience in interacting ... Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of… more
    Bristol Myers Squibb (09/23/24)
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  • Associate Director , Global Patient…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    The Associate Director , Safety Scientist in Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical ... and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments. + Ability to work… more
    Regeneron Pharmaceuticals (07/27/24)
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  • Associate Director , Regulatory…

    Bristol Myers Squibb (Madison, NJ)
    …synopses and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol ... coordination with clinical plans and marketing objectives. + Experience with clinical trial assays (CTA) in drug clinical trials in communicating between… more
    Bristol Myers Squibb (07/19/24)
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