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RBW Consulting

Pharmacovigilance Manager

RBW Consulting Woking
32 - 40 hour
new


Show Recently closed jobs

    RBW Consulting

    Pharmacovigilance Manager

    RBW Consulting Woking
    32 - 40 hour
    new
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    Pharmacovigilance & Scientific Information Manager

    I'm partnering with a long-standing client that we've successfully supported across the business for a number of years. What continues to stand out is the culture: a genuinely collaborative environment, small teams, approachable leadership, and the opportunity to have real influence. This isn't a large corporate structure where you're one of many. Instead, you'll work directly with international affiliates in a visible function that offers high potential.

    As Pharmacovigilance & Scientific Information Manager, you'll take ownership of PV activities across the UK & Ireland, acting as the local PV lead and UK Contact Person (NCPP) while leading a small team. The role offers an excellent blend of strategic responsibility and hands-on involvement, giving you the opportunity to work across pharmacovigilance, scientific information, inspections, compliance, and stakeholder management on a daily basis.

    What you'll be doing

    * Leading Pharmacovigilance activities across the UK & Ireland.

    * Acting as the UK Contact Person for Pharmacovigilance (NCPP).

    * Managing and developing a small Scientific Affairs team.

    * Working closely with global PV and Medical Affairs colleagues.

    * Maintaining oversight of Medical Information activities.

    * Supporting inspections, audits, compliance, and continuous improvement initiatives.

    What we're looking for

    * Strong Pharmacovigilance experience within the pharmaceutical industry.

    * Solid understanding of UK PV regulations, MHRA requirements, and GVP.

    * Previous people management or team leadership experience is essential – even if of small teams focusing on coaching and development

    * Experience in scientific/medical information desirable

    * Portfolio experience is less important – but experience (or a desire and capability) to deal with a large portfolio is key

    * Confidence working across multiple stakeholders and international teams.

    * A proactive, hands-on approach and the ability to thrive in a collaborative environment.

    For further details, please contact Mark Bux-Ryan.

    PV, pharmacovigilance, medical, scientific, information, safety, drug, adverse, event, MHRA, regulatory, leader, manager, supervisor, head, affairs
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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