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Global digital lead – medical, regulatory & pharmacovigilance platforms

L'Ametlla del Vallès
Planet Pharma
Publicada el 30 mayo
Descripción

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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