Oncology Regulatory Affairs Director

2 days ago


London, Greater London, United Kingdom GlaxoSmithKline Full time

About the Opportunity

We are seeking a highly skilled Associate Director to join our Oncology Therapeutic Group team at GlaxoSmithKline. As an Associate Director, you will play a critical role in ensuring the development and execution of global and/or regional regulatory strategies for assigned assets.

With a strong background in regulatory affairs, you will work closely with cross-functional teams to ensure compliance with internal processes and policies, as well as relevant regulatory requirements. Your expertise will be essential in delivering the best possible labelling that meets the Medicine Profile, commensurate with available data.

Key Responsibilities:

  • Develop and execute regional regulatory strategies in alignment with global objectives
  • Collaborate with the Early/Medicine Development Team (EDT/MDT) and Global Regulatory Lead (GRL) to ensure robust regulatory strategies support product development programs
  • Lead interactions with local/regional regulatory authorities to secure optimal labelling
  • Proactively develop regulatory strategies considering global needs while prioritizing local market requirements
  • Ensure compliance with global/regional requirements throughout the product life cycle

What We Offer

We offer a competitive salary of $140,000 - $180,000 per year, depending on experience. Our agile working culture provides flexibility to balance work and personal life. We also offer comprehensive benefits, including health insurance, retirement plans, and paid time off.



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