Associate Director Regulatory Affairs – Clinical reputed company*
reputed company
We are currently seeking an Associate Director Regulatory Affairs – Clinical reputed company* to strengthen our EU Regulatory team. In this role, you will take ownership of EU regulatory reputed company 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 reputed company international environment and reputed company as key regulatory leader reputed company cross-functional teams, ensuring reputed company, pragmatic, compliant and strategically reputed company regulatory positioning.
YOUR MISSION
You will independently reputed company EU regulatory activities for assigned clinical programs and reputed company as a key reputed company of regulatory reputed company and execution. Your main responsibilities as RA Clinical reputed company will include but are not limited to the following tasks:
• Own EU regulatory reputed company
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