• Director , GRA Strategy & Planning

    J&J Family of Companies (Providence, RI)
    …+ Basic understanding of regulatory affairs policies/guidelines and processes, and global regulatory trends + Good understanding of R&D and commercial ... Director , GRA Strategy & Planning - 2406186809W **Description**...plus **Experience and Skills:** **Required:** + 10 years in global pharmaceutical/biotechnology industry + 3 years in regulatory more
    J&J Family of Companies (05/17/24)
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  • Medical Director / Sr. Med Director

    J&J Family of Companies (Providence, RI)
    …+ Works in close partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health ... Medical Director / Sr. Med Director , Clinical Research...of clinical research studies that are part of a global compound development program. Responsibilities include: + Directs Managers… more
    J&J Family of Companies (06/01/24)
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  • Director , Executive Compensation…

    Xerox (Providence, RI)
    global guidelines, budgets, collateral materials for planning managers, global legal/ regulatory compliance, CEO approval process, participant communications). ... Director , Executive Compensation and Equity Administration **General Information**...COE. Reporting to the Vice President of Executive & Global Compensation, this role will oversee the design, development,… more
    Xerox (05/20/24)
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  • Director , Quantitative Pharmacology…

    Merck (Providence, RI)
    …including proportional hazards models. + Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics in ... **Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Director . QP2-IO team is part of the Global...+ Experience in IND, NDA and other submissions to global regulatory agencies. + Skills in experimental… more
    Merck (05/10/24)
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  • Associate Director - Pharmacometrics

    Merck (Providence, RI)
    …pharmacometric analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics, authoring ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced… more
    Merck (05/02/24)
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  • Associate Director , Clinical Quality…

    Merck (Providence, RI)
    …(QCI) colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) ... the global inspection tracking system that tracks all GCP Regulatory Health Authority inspections, findings, responses and Corrective Action and Preventive… more
    Merck (05/29/24)
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  • Director - Pharmacometrics, Quantitative…

    Merck (Providence, RI)
    …coaching/guidance to individual contributors. . Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics, ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced… more
    Merck (05/08/24)
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  • Associate Director , Clinical Trial…

    J&J Family of Companies (Providence, RI)
    Associate Director , Clinical Trial Learning & Training - 2406187889W **Description** Johnson & Johnson is recruiting for an **Associate Director , Clinical Trial ... health for humanity. Learn more at https://www.jnj.com/ . The Associate Director is responsible for deploying organizational training strategy and delivery across… more
    J&J Family of Companies (05/29/24)
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  • Market Research Associate Director

    Wolters Kluwer (Providence, RI)
    Wolters Kluwer is a global leader in professional information services that combines deep domain knowledge with specialized technology. Our portfolio offers software ... to help save lives, improve the way we do business, build better judicial and regulatory systems. We help them get it right. **Who We Are: Wolters Kluwer: The world… more
    Wolters Kluwer (04/27/24)
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  • Associate Director , Combination Product…

    Merck (Providence, RI)
    …and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible for independent ... reviewing and approving medical device/combination product documentation to support regulatory filings and audits of data, policies, procedures, and systems… more
    Merck (05/31/24)
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