Global Regulatory Strategy Director

GlaxoSmithKline; Upper Providence (Delaware County); Híbrido; USD 172 000 - 286 000; Tempo integral

Resumo da oferta

GlaxoSmithKline is seeking an experienced regulatory leader to join our Global Regulatory Strategy organization, supporting the Respiratory, Immunology and Inflammation portfolio. This role offers hybrid work options in the UK, US or Belgium and requires coordinating global regulatory activities across teams and geographies.

You will lead health authority discussions, develop evidence-based regulatory plans, and ensure submission readiness while aligning with development programs and market

Qualificações

• Bachelor's degree or equivalent in biological/health sciences.
• Significant regulatory-affairs experience across pharma development and lifecycle.
• Experience developing and delivering regulatory strategies for development programmes.
• Experience leading regulatory submission and approval activities.
• Track record of regulatory interactions with health authorities.

Responsabilidades

• Develop and execute global/regional regulatory strategies for Respiratory, Immunology and Inflammation assets.
• Ensure regulatory strategy aligns with development plans and market requirements.
• Lead health-authority interactions, submissions, and milestone meetings.
• Coordinate regulatory activities across functions and geographies.
• Provide regulatory leadership within cross-functional matrix teams.

Conhecimentos

Regulatory leadership

Cross-functional leadership

Strategic regulatory planning

Regulatory submissions

Influencing stakeholders

Formação académica

Bachelor's degree in biological science or related

Master's degree or PhD preferred

Descrição da oferta de emprego

GlaxoSmithKline is seeking an experienced regulatory leader to join our Global Regulatory Strategy organization, supporting the Respiratory, Immunology and Inflammation portfolio. This role offers hybrid work options in the UK, US or Belgium and requires coordinating global regulatory activities across teams and geographies.

You will lead health authority discussions, develop evidence-based regulatory plans, and ensure submission readiness while aligning with development programs and market