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  • Posted: Dec 2, 2020
    Deadline: Not specified
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    Novartis is a global healthcare company based in Switzerland that provides solutions to the evolving needs of patients worldwide.
    Read more about this company

     

    Regulatory Affairs Head, English West Africa

    Ref Id: 308121BR
    Division: Global Drug Development
    Business Unit: REG AFFAIRS GDD
    Functional Area: Research & Development
    Employment Type: Regular
    Shift Work: No

    Job Description

    • Is responsible for implementing regulatory strategy and managing operational activities for assigned major/ large regions.
    • Provides input into global regulatory strategy and contributes to Regulatory Functional Plan (RFP) and Seed Document, or their equivalents, including identification of gaps or risks in global strategic plan for assigned regions.
    • Partners with regions to align on regulatory strategy in order to fulfil business objectives.
    • Implements RFP across assigned regions.
    • Determines requirements and sets objectives for Health Authority (HA) interactions with DRA GPT representative and/or GTAL.
    • Facilitates preparation and finalization of briefing books and contributes to preparation of summary documents. -Develops and implements plans for timely response to HA requests and coordinates responses.
    • May serve as local HA liaison depending on location (e.g., FDA or EMA).
    • Drives coordination, planning, and submission of dossiers in assigned regions worldwide.
    • Review of global dossier summary documents.
    • Develops and implements plans to avoid/minimize clock stops during submission review.
    • Reviews, approves and submits Clinical Trial Applications (CTAs) and Investigational New Drugs (INDs).
    • Reviews and submits Risk Management Plans.
    • May lead negotiations for regional approvals independently or with DRA GPT representative and/or GTAL.
    • Responsible for facilitating timely submission and approval of dossier with HAs under the guidance of the DRA GPT representative and/or GTAL.
    • Contributes to and often leads the development of departmental goals and objectives.

    Minimum Requirements
    Educational Qualification:

    • Pharm D, Master in Life Sciences degree. PhD or Higher Degree or equivalent experience desirable

    Required Experience:

    • Operations Management and Execution Project Management Representing the organization Functional Breadth Cross Cultural Experience

    Method of Application

    Interested and qualified? Go to Novartis International AG on www.novartis.com to apply

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