Global Labelling Associate Director, Content

About the role

The Global Labelling Associate Director will shape and maintain labelling strategies for cardiovascular, renal and metabolism products throughout their lifecycle, ensuring alignment with regulatory expectations and market needs.

Key responsibilities

• Develop and maintain global labelling strategies and content for established products.
• Lead cross‑functional discussions to align on strategy, content and key product claims.
• Drive creation and upkeep of core and major market labelling documents.
• Present labelling recommendations to governance bodies and project teams.
• Anticipate emerging labelling risks and devise mitigation plans.
• Support health authority interactions with evidence‑based responses and negotiation strategies.
• Mentor colleagues and contribute to continuous improvement and inspection readiness.

Required profile

• Degree in a scientific discipline with strong understanding of pharmaceutical development and regulatory requirements.
• Experience developing and maintaining global labelling content 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 across major health authorities.
• Proven ability to collaborate across multidisciplinary teams and influence stakeholders.

What we offer

• Annual base salary range £67,900 – £126,100, plus performance‑based bonus.
• Competitive benefits including insurance, retirement plans, wellbeing resources and flexible hybrid working.
• Minimum 14 weeks paid parental leave and potential company vehicle or car allowance.
• Commitment to pay equity, diversity and inclusion.