Global Digital Lead – Medical, Regulatory & Pharmacovigilance Platforms

  • Tiempo completo
  • catalonia

Planet Pharma

Global Digital Lead – Medical, Regulatory & Pharmacovigilance Platforms

An innovative global biopharmaceutical organisation with a rapidly expanding R&D pipeline is seeking a Global Digital Lead to drive the strategy, implementation, and optimisation of enterprise digital platforms across Medical Affairs, Regulatory Affairs, and Pharmacovigilance functions.

This is a high-impact leadership opportunity for someone passionate about science, digital transformation, and building scalable global solutions in a highly collaborative environment.

The Opportunity

You will lead the evolution of critical business platforms supporting global scientific and regulatory operations, acting as the bridge between business stakeholders and technology teams/vendors.

The role combines:

  • Digital strategy
  • Product ownership
  • Stakeholder leadership
  • Platform governance
  • Team management
  • Global transformation delivery

You will manage a small international team while influencing senior stakeholders across Medical Affairs, Regulatory Affairs, PV, Quality, and Digital functions globally.

Key Responsibilities

  • Define and execute the digital platform roadmap across Medical Affairs, Regulatory Affairs, and PV
  • Lead implementation and optimisation of enterprise systems and business-critical digital solutions
  • Partner with scientific and technical stakeholders to align business priorities with digital capabilities
  • Drive compliance, validation, and governance standards including 21 CFR Part 11
  • Manage external vendors and technology partners
  • Lead continuous improvement initiatives focused on operational efficiency and data-driven decision making
  • Mentor and develop a team of up to 5 direct reports

What We’re Looking For

  • Strong scientific background within pharma/biotech
  • Proven experience leading global digital or product initiatives within Medical Affairs, Regulatory Affairs, and/or Pharmacovigilance
  • Hands-on experience with enterprise platforms such as:
  • Veeva RIMS
  • ARIS / LifeSphere
  • Medical Affairs platforms
  • Strong understanding of regulated environments, validation, and compliance requirements
  • Experience managing cross-functional global stakeholders in matrix organisations
  • Excellent communication and influencing skills
  • Leadership mindset with a proactive, entrepreneurial approach

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