Regulatory Affairs Director

2 weeks ago


Copenhagen, Copenhagen, Denmark Genmab Full time

About the Position

We are seeking a highly skilled Regulatory Affairs professional to join our team as an Associate Director, Global Regulatory Affairs Project Lead. In this role, you will have the opportunity to utilize your expertise to drive regulatory compliance and quality in clinical trials.

Responsibilities

  • Drive regulatory compliance and quality in clinical trials.
  • Develop and execute EU/ROW regulatory strategies for assigned projects.
  • Prepare and submit regulatory documents, such as Briefing Packages, ODDs, and PIPs.
  • Cultivate strong relationships with cross-functional teams to ensure alignment and effective communication.

About Our Culture

  • We value diversity, equity, and inclusion in our workplace culture.
  • We prioritize collaboration and open communication among team members.


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