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    Regulatory Affairs Manager - England, United Kingdom - ICON Strategic Solutions

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    Description
    Regulatory Affairs Manager- (EU CTR) Homebased in UK/Ireland Only

    Due to recent success within one our Innovative Biotech Clients I am recruiting for a Regulatory Affairs manager at ICON - Working in a client-dedicated yet fully embedded role ICON's Regulatory Strategy group, you will lead or contribute to the development and execution of the drug development strategy of our client's new therapeutics.

    The ideal candidate would have experience in EU CTR and making regulatory submissions via CTIS. You will be supporting the EU regulatory team with planning and executing regulatory submissions for allocated studies.

    Prepare, review and support submissions to HA/Regional CTA Hub, in order to obtain all necessary authorizations/approvals pertaining to the clinical trial conduct.

    Expert knowledge of current CTA guidelines and regulations is preferred, as well as the ability to understand new guidelines and regulations as they are issued by major regulatory authorities in the region.

    Adaptable, collaborative and an expert in regulatory CTA's.

    Here at Icon we want our employees to succeed and ensure that they are set up for this success through constant training, development and support.

    B.Sc is in Pharmacy, Life Sciences, Business or Information Technology (desirable); Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards


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