Regulatory Affairs Expert

1 week ago


Copenhagen, Copenhagen, Denmark Genmab Full time
About the Role

We are seeking a highly skilled Associate Director, Global Regulatory Affairs Project Lead to join our team at Genmab. This individual will be responsible for representing RA in the Clinical Trial Teams and ensuring regulatory oversight and progress of multiple clinical trial submission activities.

The successful candidate will work closely with the CRO and internal stakeholders to ensure regulatory compliance and progress of clinical trials in EU/ROW. They will also be responsible for developing and executing the EU/ROW strategy for assigned projects and leading the preparation of strategic regulatory documents.

This is an excellent opportunity for a motivated and experienced professional to join our dynamic team and contribute to the development of innovative cancer treatments.



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