Associate Director Regulatory Affairs – Clinical Lead*
OVERVIEW
We are currently seeking an Associate Director Regulatory Affairs – Clinical Lead* to strengthen our EU Regulatory team. In this role, you will take ownership of EU regulatory strategy and execution for innovative oncology biopharmaceutical programs, including ATMPs, across early and late-stage development.
You will work in Tübingen, Munich or remote (Germany) in a highly collaborative international environment and act as key regulatory leader within cross-functional teams, ensuring clear, pragmatic, compliant and strategically aligned regulatory positioning.
YOUR MISSION
You will independently lead EU regulatory activities for assigned clinical programs and act as a key driver of regulatory strategy and execution. Your main responsibilities as RA Clinical Lead will include but are not limited to the following tasks:
• Own EU regulatory strategy
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