Clinical Trial Manager - European Union - i-Pharm Consulting

    i-Pharm Consulting
    i-Pharm Consulting European Union

    1 hari yang lalu

    Deskripsi

    Clinical Trial Manager (CTM)

    Fully Remote – UK or Europe

    Permanent Opportunity | April Start

    We are partnering with a highly respected, mid-sized CRO with a long-standing reputation for delivering high-quality clinical research across Europe. Following recent strategic growth and acquisitions, the organisation now benefits from global backing while maintaining its collaborative, family-oriented culture and personal approach to clients.

    With a significant project expected to commence shortly, they are seeking an experienced Clinical Trial Manager to join their team for an April start.

    The Opportunity:

    As a Clinical Trial Manager , you will oversee the operational delivery of Phase I–III clinical trials across multiple sites and potentially multiple countries. This is an individual contributor role with no direct line management; however, you will provide operational oversight and guidance to CRAs and Clinical Trial Coordinators within a matrix structure.

    Key Responsibilities:


    • Lead the operational execution of clinical trials from start-up through close-out


    • Ensure studies are delivered on time, within budget, and in compliance with ICH-GCP and regulatory requirements


    • Oversee timelines, study plans, vendor management, and risk mitigation strategies


    • Act as escalation point for CRAs and study teams


    • Manage sponsor communication and reporting


    • Maintain inspection readiness and TMF oversight

    Candidate Profile:


    • Experience as a Clinical Trial Manager, Clinical Study Manager, or a strong Lead CRA with operational project responsibility


    • Experience managing multicentre studies (global exposure advantageous)


    • Strong understanding of budgets, forecasting, and vendor oversight


    • Confident in sponsor-facing interactions and cross-functional leadership


    • Solid knowledge of ICH-GCP and regulatory requirements

    Why Join?


    • Mid-sized CRO where you are valued and not just a number


    • Supportive, experienced clinical leadership team


    • Strong retention and genuine internal progression opportunities


    • Competitive Salary package


    • Fully remote working model across the UK and Europe

    If you would like to learn more, please reach out for a discussion.


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