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Closed
H

Regulatory Affairs Consultant EU and US

Hays Life Sciences Uxbridge
50 to 60
32 - 40 hour
new


Show Recently closed jobs

    Closed vacancy

    You are currently viewing a closed vacancy. You can no longer apply for this vacancy.

    H

    Regulatory Affairs Consultant EU and US

    Closed
    Hays Life Sciences Uxbridge
    50 to 60
    32 - 40 hour
    new
    Status Closed
    Applications are no longer accepted

    What we ask

    Education

    No minimum education required

    What we offer

    Salary
    £50 to £60
    Hours
    32 to 40 hours per week
    Employment type
    contract

    Job description

    Your new company
    A leading Regulatory Affairs consultancy looking for an experienced regulatory professional to support one of the Regulatory Strategy Leads across EU and US development activities. The role requires a hands-on individual with a strong clinical regulatory background, operational submission experience, and working knowledge of both EMA centralised procedures and FDA regulatory requirements.
    This is a remote, outside IR35 contract job in Regulatory Affairs.

    Your new role
    Regulatory Operational Support

    Provide operational regulatory support to the assigned Regulatory Strategy Lead.
    Support EU and US development regulatory activities across ongoing programmes.
    Coordinate regulatory timelines, deliverables, and submission readiness activities.
    Track and manage regulatory actions, commitments, and submission milestones.
    Support internal governance and cross-functional coordination activities.
    Clinical Regulatory Documentation

    Perform hands-on preparation, review, formatting, and maintenance of regulatory documentation.
    Support updates to clinical and regulatory documents in line with authority expectations.
    Coordinate document version control and ensure submission-ready quality standards.
    Support authoring coordination activities across internal stakeholders and external vendors where applicable.
    EU Centralised Procedure Support

    Provide operational support for EMA centralised procedure activities.
    Assist with dossier compilation and submission coordination.
    Support life cycle management activities associated with development submissions.
    Ensure alignment of submission documentation with EU regulatory requirements and timelines.
    FDA Regulatory Support

    Support US regulatory operational activities and FDA-related documentation requirements.
    Assist with submission preparation and document management activities for US filings.
    Coordinate responses, updates, and submission components in collaboration with the Regulatory Strategy Lead.

    What you'll need to succeed

    What you'll get in return
    Remote working, outside IR35 rate

    What you need to do now
    If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
    If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career
    Salary description

    £50.00 - £60.00 per hour

    Applications are no longer accepted
    Applications are no longer accepted

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