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    Full-time Writer - United Kingdom - Carrot Pharma Recruitment

    Carrot Pharma Recruitment
    Carrot Pharma Recruitment United Kingdom

    3 weeks ago

    Default job background
    Full time
    Description
    Regulatory Writer – International Consultancy – Remote (UK based) - £negotiable


    This is an exciting time to join an expanding, highly successful Consultancy on a permanent basis based in South Manchester / Cheshire, however the role can also have some remote working.

    They offer excellent training and development opportunities as well as great career progression and an excellent work/life balance.

    This role is based in Cheshire but can also involve remote working (UK only) and can also offer part time options if required (30 hours/4 days).


    An independently owned, international consultancy is now recruiting for a Regulatory Writer to join them on a full or part time basis, based remotely in the UK.

    Excellent career progression opportunities

    Great training and development

    Exciting and innovative projects


    The Regulatory Writer will have the opportunity to work with well known, innovative pharmaceutical companies across a range of therapy areas.

    Plan and deliver regulatory submissions on behalf of pharmaceutical clients

    Prepare clinical regulatory documents across multiple therapy areas

    Evaluate scientific data

    Work on projects independently as well as group projects

    To apply for this role as Regulatory Writer our client is hoping for someone with the following skills and experience

    Ample regulatory writing experience within a pharmaceutical company, CRO or Consultancy

    Experience writing clinical regulatory documents to a high standard

    Experience authoring regulatory documentation such as CTD modules, response documents and regulatory briefing documents

    Degree educated in life sciences / pharmaceutical science


    This Regulatory Writer role is one not to be missed; it encompasses the opportunity to work in a fast-paced environment on new and exciting projects.

    To discuss this role or other live Regulatory Affairs jobs further, please submit your current CV or give me a call today.

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