• Associate Director , Clinical

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    … and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix ... clinical studies and programs. As an Associate Director a typical day may include...in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical more
    Regeneron Pharmaceuticals (01/29/25)
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  • Associate Director , Clinical

    Gilead Sciences, Inc. (Parsippany, NJ)
    …their aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director , Clinical Pharmacology - Virology** **_*This is ... and study sites to implement and monitor clinical pharmacology studies . Addresses clinical ...regulations, ICH guidelines, and GCP governing the conduct of clinical studies . Has significant knowledge of pharmaceutical… more
    Gilead Sciences, Inc. (03/04/25)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress. + Manages all aspects of Quality ... quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable...with senior level management, external vendors, collaboration partners and clinical study personnel for clinical more
    Regeneron Pharmaceuticals (01/10/25)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Develops biomarker strategy in collaboration with Translational Medicine/Clin Pharm; May act as Clinical study leader (CSL) + Study Planning and Execution: ... Provides medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams. **Responsibilities** + Study Strategy:… more
    Daiichi Sankyo Inc. (02/14/25)
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  • Associate Director , Clinical

    Merck (Rahway, NJ)
    …operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...ensures proper allocation of drug product as needed across studies within assigned program(s). + Responsible for identifying significant… more
    Merck (03/14/25)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Madison, NJ)
    …and success of the BMS R&D pipeline. This role reports to the Director , Clinical Data Management or Associate Director , Clinical Data Management ... is responsible for: **Project Management and Leadership** + Provides clinical data management leadership within the study ...Provides clinical data management leadership within the study team to align on and drive data collection… more
    Bristol Myers Squibb (03/16/25)
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  • Associate Director / Director

    AbbVie (Florham Park, NJ)
    … development projects. A visible and collaborative role, the Associate Director / Director works in partnership with clinical and regulatory experts ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director / Director , Statistics (Dermatology) provides scientific… more
    AbbVie (03/04/25)
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  • Senior Clinical Study Manager

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic... trial performance and quality metrics and share with study team, Operations Program Lead, and Sr. Director more
    Daiichi Sankyo Inc. (02/05/25)
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  • Associate Principal Scientist…

    Merck (Rahway, NJ)
    **Job Description** **Title: Associate Principal Scientist/ Associate Director , Outcomes Research** **Role Summary** + Under the guidance of a senior leader, ... an Associate Principal Scientist/ Associate Director , has...In collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires,… more
    Merck (03/20/25)
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  • Associate Director , Quality Risk…

    Bristol Myers Squibb (Summit, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . Position Summary The Associate Director , RBQM - HOCT, ICN will mainly be responsible ... and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and...compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to ensure… more
    Bristol Myers Squibb (03/20/25)
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  • Associate Director , Oncology…

    Bristol Myers Squibb (Madison, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Oncology & Hematology, Medical Evidence Generation will: + ... concepts to full proposals and aid in site assessment/recommendation, facilitation of study design, presentation to governance in partnership with disease area leads… more
    Bristol Myers Squibb (03/04/25)
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  • Associate Director , Product…

    Taiho Oncology (Princeton, NJ)
    Associate Director , Product Development Princeton, NJ, USA Req #448 Thursday, March 6, 2025 Looking for a chance to make a meaningful difference in the oncology ... responsible not only for product development but also support clinical studies , commercialization and life-cycle management. You...is the role for you. Position Summary: + The Associate Director , Product Development will be responsible… more
    Taiho Oncology (03/07/25)
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  • Associate Director , Therapeutic…

    Bristol Myers Squibb (Summit, NJ)
    …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... protocols using data and information from discovery phase, non- clinical and clinical studies +...that GxP follow-up CAPA activities are completed + Oversee study centers, countries, investigators and connect with PV, Medical… more
    Bristol Myers Squibb (03/20/25)
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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 ... trial design, analysis planning, study results presentation and interpretation, clinical study report authoring, regulatory submissions and publications. +… more
    Bristol Myers Squibb (02/22/25)
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  • Associate Director , PV Medical…

    Taiho Oncology (Princeton, NJ)
    Associate Director , PV Medical Surveillance Princeton, NJ, USA Req #435 Tuesday, February 11, 2025 Looking for a chance to make a meaningful difference in the ... and written communication, planning, organization, with knowledge of the investigational clinical study and post-marketing settings. + Working knowledge of… more
    Taiho Oncology (02/11/25)
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  • Associate Director , PV Sciences

    Taiho Oncology (Princeton, NJ)
    Associate Director , PV Sciences Princeton, NJ, USA Req #444 Thursday, February 27, 2025 Looking for a chance to make a meaningful difference in the oncology ... Value Proposition: Embark on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the forefront of pharmacovigilance… more
    Taiho Oncology (03/04/25)
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  • Associate Director , Quantitative…

    Merck (Rahway, NJ)
    …**Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global ... 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 (03/14/25)
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  • Associate Principal Scientist…

    Merck (Rahway, NJ)
    …programs. + In collaboration with internal teams and external partners, design studies , author study protocols, develop measurement questionnaires, case report ... to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and...forms, data analysis plans, final study reports, scientific presentations, and publications.… more
    Merck (03/20/25)
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  • Associate Director , Quality Control…

    BeiGene (Pennington, NJ)
    **_General Description:_** Establish a stability program in Quality Control for clinical and commercial phase biologics products in accordance to FDA/EU regulations, ... and BeiGene processes and procedures. Oversee and manage stability studies to deliver scientifically sound GMP test data in...+ Establish and manage the QC stability program for clinical and commercial phase biologics products. + Ensure timely… more
    BeiGene (02/06/25)
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  • Associate Director , Statistical…

    Bristol Myers Squibb (Princeton, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director of Statistical Methodology and Innovation works closely ... rigor and innovation, operational feasibility, and resource efficiency across the BMS portfolio. Associate Director of Stat Methodology role will be involved in… more
    Bristol Myers Squibb (02/12/25)
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