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Director of Global Regulatory Affairs and Precision Medicine

vor 2 Monaten


Zug, Zug, Schweiz 1925 GlaxoSmithKline LLC Vollzeit
Job Summary

We are seeking a highly skilled and experienced professional to lead our global regulatory affairs and precision medicine efforts. As Director of Global Regulatory Affairs and Precision Medicine, you will be responsible for developing and executing regulatory strategies for precision medicine and digital health assets across our therapeutic portfolio.

Main Responsibilities

  • Develop and execute global regulatory strategies for precision medicine and digital health assets.
  • Ensure compliance with regulatory requirements at all stages of product life, from C2MD to launch.
  • Lead regulatory interactions and review processes for GSK.
  • Collaborate with cross-functional teams to advance regulatory submissions and approvals.
  • Provide expert guidance on regulatory matters related to precision medicine and digital health.

Requirements

  • Masters degree in biological science, healthcare science, or engineering.
  • Minimum 5 years of experience in regulatory affairs, with a focus on precision medicine and digital health.
  • Proven track record of leading global regulatory strategies and submissions.
  • Excellent communication and leadership skills.

What We Offer

At 1925 GlaxoSmithKline LLC, we offer a competitive compensation package, comprehensive benefits, and a dynamic work environment that fosters growth and development.