Regulatory Affairs Director

5 days ago


Copenhagen, Copenhagen, Denmark Genmab Full time

About the Job

We are seeking a highly motivated and self-driven individual to lead the development and execution of the EU/ROW regulatory strategy for assigned projects. As a Senior Regulatory Affairs Manager, you will be responsible for representing RA in the Clinical Trial Teams and ensuring oversight and progress of multiple clinical trial submission activities.

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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