Clinical Regulatory Expert - Lisbon - beBeeRegulatory

    beBeeRegulatory
    beBeeRegulatory Lisbon

    há 1 semana

    Tempo integral

    Título do emprego: Principal Medical Writer sponsor dedicated

    Descrição

    At our organization, we are seeking an expert contributor to join a collaborative framework where you will work closely with one sponsor and their team.

    Job Description:

    • You will leverage your expertise to develop complex clinical regulatory documents including Clinical Study Protocols, Investigator Brochures, clinical summary modules, overview documents in CTD/eCTD format worldwide.

    Responsibilities include writing, managing and collaborating with stakeholders through document development. You will also manage projects by facilitating decision-making processes that propel the document cycle forward.
    A PhD or Master's degree along with at least 6 years of experience in eCTD submission as well as leadership skills is required for this role.Career Opportunities And Aspirations: To have control over personal growth while making an impact in a collaborative workspace that joins exceptional talented individuals passionate about revolutionizing process delivering swift life-changing ideas therapies patients ],


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