Pharmacovigilance Manager

Company: Fusion Group

  • Location: United Kingdom
  • Work mode: Remote
  • Seniority: Senior
  • Employment type: Full-time
  • Posted: Yesterday
  • Offer language: English

Job description

Pharmacovigilance Manager

Location: Remote, UK.

Contract Type: Permanent, full time.

We’re looking for a Pharmacovigilance Manager to join a growing PV team, playing a key role in combining strategic PV oversight with client engagement and programme governance.

The role

As Pharmacovigilance Manager, you’ll take ownership of the PV strategy across multiple global programmes, working closely with clients and internal stakeholders to develop and implement compliant, scalable safety frameworks across multiple regions.

Key responsibilities

  • Take ownership of establishing effective pharmacovigilance models for individual programme needs, client requirements and varying international regulatory landscapes.
  • Advise on the interpretation and application of safety obligations, including reporting requirements, oversight arrangements and local regulatory expectations across different territories.
  • Play an active role in developing and enhancing the organisation's pharmacovigilance capabilities, contributing to new service propositions and wider business growth initiatives.
  • Evaluate the safety and compliance implications associated with programme developments, including entry into new markets, alternative access pathways and changes to the populations being supported.
  • Oversee preparation, submissions, periodic reports, line listings and safety summaries.
  • Lead the assessment and implementation of safety-related programme changes, ensuring regulatory obligations continue to be met while maintaining continuity of service delivery.
  • Partner cross functionally with teams to identify opportunities and design tailored solutions.
  • Provide strategic oversight for programme implementation and ongoing safety management

What we’re looking for

  • 5+ years experience within a pharmacovigilance environment
  • EAP experience is advantageous
  • Analytical thinker
  • A good understanding of global regulatory requirements, safety reporting and compliance.

Why apply?

This role offers the opportunity to work within a specialist environment where you’ll gain exposure to program design, strategic pharmacovigilance, client engagement & delivery of EAP's.

You’ll join a collaborative team with excellent opportunities for professional development and career progression.

If you’re looking for a leadership pharmacovigilance role where you can make a real impact on global EAP operations, we’d love to hear from you.

Courses that can help you get this job

  • Course matchperiodic reports

    SUSAR, DSUR, PLL reports

    SUSAR, DSUR, PLL reports

    PharmacovigilanceClinical Trials
    Rating: 4.29 (7 reviews)Total duration: 1h 38m
    Monika Nowak, Marek Hurda
    Certified by:Certified by

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