Director, Global Regulatory Affairs Strategy and Development

5 days ago


Copenhagen, Copenhagen, Denmark Genmab Full time

About Genmab

Genmab is an international biotechnology company committed to improving the lives of patients through innovative antibody therapeutics. We leverage translational research and data sciences to develop next-generation antibody technology platforms, including bispecific T-cell engagers, immune checkpoint modulators, effector function enhanced antibodies, and antibody-drug conjugates.

The Role and Department

In this role, you will join our Global Regulatory Affairs organization, assuming responsibility for the EU/ROW regulatory strategy, closely collaborating with the Global Regulatory Team on one or multiple compounds in early or late-stage development.

Key Responsibilities

  • Act as EU/ROW regulatory lead and EMA contact person for assigned project(s)
  • Represent RA in the Clinical Trial Teams and ensure oversight and progress of multiple clinical trial submission activities
  • Evaluate competitive landscape and various regulatory mechanisms to optimize product development and expedite the path to market in EU/ROW

Requirements

  • A minimum of Bachelor's degree or equivalent in scientific discipline or health-related field
  • Minimum of 7-8 years of experience in Regulatory Affairs, preferably in development phase
  • Significant experience in proactively planning and executing complex clinical submission strategies
  • Solid understanding of drug development and EU regulatory mechanisms
  • Prior experience leading health authority meetings with the EMA or other health authorities, as well as experience with PIPs
  • Strong project management skills


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