Associate Director, Oncology Regulatory Strategy

18 hours ago


Collegeville, Pennsylvania, United States GSK Full time
Job Summary

We are seeking an experienced Associate Director to lead our Oncology Regulatory Strategy team. The successful candidate will be responsible for developing and implementing regional regulatory strategies to support the development and launch of new oncology products.

Key Responsibilities
  • Develop and implement regional regulatory strategies to support the development and launch of new oncology products.
  • Lead interactions with local and regional regulatory authorities to ensure compliance with global and regional requirements.
  • Collaborate with cross-functional teams, including commercial and medical affairs, to ensure alignment and effective communication.
  • Provide regulatory expertise and guidance to support the development and launch of new oncology products.
  • Stay up-to-date with regulatory requirements and trends in the oncology space to ensure our strategies remain effective and compliant.
Requirements
  • Bachelor's degree in a relevant field, such as biological or healthcare science.
  • 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 collaboration skills, with the ability to work effectively with cross-functional teams.
  • Strong knowledge of regulatory requirements and trends in the oncology space.
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 professional looking for a new challenge, we encourage you to apply.



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