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    Senior Manager Regulatory Affairs Writing - cambridge, United Kingdom - Pharma Partners Recruitment Ltd

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    Pharmaceutical / Bio-tech
    Description

    Job title: Senior Manager Regulatory Affairs Writing

    A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. The role will play a pivotal role in the clinical development team. You will lead a team responsible for developing the content for submissions to both US and EU regulatory agencies.

    Responsibilities:

    • scientific contribution to the development of medical, regulatory and clinical documents to support development programmes. This includes (not limited to) clinical study protocols, investigator brochures, non-clinical summaries, briefing documents, safety/efficacy summaries and clinical study reports.
    • and manage the medical and regulatory writing team along with use of external writing resources when necessary
    • and coordinate the development of cross-functional documents to ensure completion to timelines.
    • and develop clinical and medical materials, ensuring that outputs are appropriately referenced and accurate in content and editorial style.

    Requirements:

    • of first degree in life sciences (or equivalent); advanced degree (e.g. PhD or Masters) preferred.
    • of writing in the field of Clinical Development within the pharmaceutical industry or contract research organisations
    • in writing for clinical trials across a range of therapeutic areas and geographies, ideally with immunology/dermatology experience
    • experience in medical communications, editing and/or publishing would be advantageous

    Salary and benefits:

    A highly competitive salary, stock options, annual bonus and wider benefits scheme is on offer

    To apply for this position or hear further details then please contact Matt Thomas via



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