• Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and strategic insights at the study team level. The Associate Director of Regulatory Writing more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …well as other research areas centered around rare diseases and immune disorders.Summary The Associate Director of Regulatory Writing is a key role ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and strategic insights at the study team level. The Associate Director of Regulatory Writing more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and guidelines, reviews and provides written assessments of relevant medical topics, and supports PV Operations' medical ...and relevant team members.Reports and Submissions: May contribute to writing minor safety sections of the NDA, CSR, and… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …implementation of sourcing strategies for a specific set of R&D categories (CRO, Medical Writing , BDM, etc..). Builds strategic plans for specific categories ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... technical knowledge based upon academic training and job experience.Strong oral and writing skill. Able to write regulatory documents in highly complex technical… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …of Global RD and PV QA organizational strategy in collaboration with the Associate Director Global Strategy and Operations and Head Global Strategy and ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...Operations. In collaboration with the Associate Director Global Strategy and Operations and… more
    HireLifeScience (09/24/24)
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  • Associate Director , Medical

    Takeda Pharmaceuticals (Trenton, NJ)
    …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Associate Director Medical Writing where you will be ... data presentation and interpretation. In addition to project responsibilities, the Associate Director , Medical Writing is responsible for non-project… more
    Takeda Pharmaceuticals (10/05/24)
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  • Associate Director / Director

    Intra-Cellular Therapies, Inc (Bedminster, NJ)
    …bipolar depression in adults as monotherapy and as adjunctive therapy. The Associate Director / Director of Medical Writing provides support for the ... documents, and responses to health authority information requests. The Associate Director / Director of Medical Writing must have experience with… more
    Intra-Cellular Therapies, Inc (09/19/24)
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  • Associate Director , Nonclinical…

    Takeda Pharmaceuticals (Trenton, NJ)
    …true to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** ... our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and...US based employees may be eligible to participate in medical , dental, vision insurance, a 401(k) plan and company… more
    Takeda Pharmaceuticals (09/19/24)
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  • Associate Director , Regulatory…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …as other research areas centered around rare diseases and immune disorders. **Summary** The Associate Director of Regulatory Writing is a key role ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and strategic insights at the study team level. The Associate Director of Regulatory Writing more
    Daiichi Sankyo Inc. (09/25/24)
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  • Associate Director , Regulatory…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …other research areas centered around rare diseases and immune disorders. **Job Summary:** The Associate Director of Regulatory Writing is a key role ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and strategic insights at the study team level. The Associate Director of Regulatory Writing more
    Daiichi Sankyo Inc. (09/05/24)
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  • Associate Director , Medical

    J&J Family of Companies (Titusville, NJ)
    Associate Director , Medical Information Scientific Engagement - 2406206238W **Description** The Associate Director , Medical Information ... experience and engagement strategies within given therapeutic areas. The Associate Director will lead and foster a...for scientific efficiency to conduct manager review. * Ensure medical writing authoring training and skillset development… more
    J&J Family of Companies (09/19/24)
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  • Associate Director , US…

    Bristol Myers Squibb (Princeton, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Associate Director , Medical Promotional Review Scientist, ... Neuropsychiatry **Location:** Princeton Pike, NJ or Madison, NJ The Associate Director , Medical Promotional Review...or the pharmaceutical industry. + Demonstrates thorough understanding of medical writing and medical review… more
    Bristol Myers Squibb (10/03/24)
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  • Associate Director of Research

    FranklinCovey (Trenton, NJ)
    …schools and institutions. To learn more, visit franklincovey.com . **Title:** Associate Director of Research **Division & Department:** Education **Status:** ... **Location:** Remote - Anywhere in the contiguous United States **Job Summary** The Associate Director of Research at FranklinCovey's Education Division is a… more
    FranklinCovey (10/01/24)
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  • Associate Director , Outsourcing…

    Taiho Oncology (Princeton, NJ)
    Associate Director , Outsourcing & Vendor Management Pleasanton, CA, USA * Princeton, NJ, USA Req #385 Friday, August 16, 2024 Looking for a chance to make a ... Proposition: Join our dynamic and expanding mid-size company in the role of Associate Director , Outsourcing and Vendor Management. Your expertise will play a… more
    Taiho Oncology (08/17/24)
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  • Associate Director , Clinical…

    AbbVie (Branchburg, NJ)
    …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Development will have global or regional ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Lead and Clinical Science Lead and Clinical Scientist. The Associate Director , Clinical Development should expect to… more
    AbbVie (09/20/24)
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  • Associate Director , Clinical Data…

    Bristol Myers Squibb (Princeton, NJ)
    …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 with ... and directly contributes to the BMS R&D pipeline. This role reports to Director or Executive Director , Head Standards Management & Steward within Clinical… more
    Bristol Myers Squibb (09/21/24)
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  • Associate Director , RA Labeling…

    J&J Family of Companies (Titusville, NJ)
    Associate Director , RA Labeling Product Leader (1 of 2) - 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate ... Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance) including at least 6 years of direct… more
    J&J Family of Companies (08/10/24)
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  • Associate Director , External Data…

    Bristol Myers Squibb (Princeton, NJ)
    …centralized monitoring for trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a leadership role with ... directly contributes to the BMS R&D pipeline. This role reports to the Director , External Data Acquisition within GDM and is a full-time, office-based position.… more
    Bristol Myers Squibb (09/24/24)
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