Associate Director, Oncology Regulatory Affairs

2 days ago


Collegeville, Pennsylvania, United States GSK Full time
Job Summary

We are seeking a highly skilled and experienced Associate Director, Oncology Regulatory Affairs to join our team at GSK. As a key member of our regulatory affairs team, you will be responsible for developing and implementing regulatory strategies to support the development and approval of oncology products.

Key Responsibilities
  • Develop and implement regulatory strategies to support the development and approval of oncology products
  • Collaborate with cross-functional teams, including clinical, medical, and commercial, to ensure regulatory compliance and optimal product labeling
  • Provide regulatory guidance and support to project teams to ensure compliance with regulatory requirements
  • Develop and maintain relationships with regulatory agencies, including the FDA and EMA
  • Stay up-to-date with regulatory developments and trends in the oncology space
Requirements
  • PhD or equivalent in a relevant field, such as regulatory affairs, pharmacology, or a related field
  • Minimum 5 years of experience in regulatory affairs, with a focus on oncology
  • Proven track record of developing and implementing successful regulatory strategies
  • Excellent communication and interpersonal skills
  • Ability to work in a fast-paced environment and prioritize multiple tasks and projects
What We Offer

We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and experienced regulatory affairs professional looking for a new challenge, we encourage you to apply.



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