Regulatory Affairs Leader
2 days ago
About the Job
We are seeking a seasoned Regulatory Affairs professional to join our Global Regulatory Affairs team. As a Senior Director, you will be responsible for the development and implementation of EU/ROW regulatory strategies for Genmab's programs across all stages of development. You will work closely with cross-functional teams to ensure an optimal development and implementation of EU/ROW regulatory strategies that enable an integrated global clinical development and commercial strategy.
The ideal candidate will have a minimum of 10 years of experience in Regulatory Affairs, with significant experience in proactively planning and implementing complex clinical submission strategies. A strong understanding of drug development and EU regulatory mechanisms is essential, with expertise in expedited development pathways such as orphan drug designation and PRIME designation.
You will be responsible for leading and mentoring a team of dedicated Regulatory Strategists with EU/ROW responsibilities. You will also interact directly with health authorities, including the EMA, and lead/participate in health authority meetings.
Requirements
- A minimum of Bachelor's degree or equivalent in scientific discipline or health-related field
- Minimum of 10 years of experience in Regulatory Affairs
- Significant experience in proactively planning and implementing complex clinical submission strategies
- Experience in leading a team of regulatory professionals
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