Global Labelling Associate Director, Content (Oncology)
On-siteDublin, Leinster, Ireland
Job Summary
Develop and maintain global labelling strategies and content for established oncology products across development and lifecycle activities. Lead cross-functional discussions to align on global labelling strategy, key product claims, and core document creation. Present recommendations to governance bodies, anticipate emerging risks, and develop mitigation and escalation plans. Support health authority interactions by preparing evidence-based responses and negotiation strategies while mentoring colleagues on inspection readiness. This role supports patient safety and regulatory compliance for medicines improving lives worldwide. Based in Dublin, Ireland, with hybrid working options available.
Required Qualifications
- Degree in a scientific discipline
- Strong understanding of pharmaceutical development and regulatory requirements
- Experience developing and maintaining global labelling content for medicinal products across the product lifecycle
- Ability to interpret clinical efficacy and safety data and translate findings into clear labelling content
- Strong knowledge of global labelling regulations and requirements across major health authorities
- Proven ability to collaborate effectively across multidisciplinary teams and influence diverse stakeholders
- Excellent planning, prioritisation, communication, and attention to detail with a focus on quality
- Must be accessible in Dublin, Ireland
- Must be willing to forego relocation support
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