EU Regulatory Lead
Vor 7 Tagen
Your role
The EU Regulatory Lead (EU RL) is responsible for the regulatory strategy and execution for their assigned projects in their EU region and respective countries. The EURL represent and provide input for the respective EU region at the GRST. The person may provide direct input to the GPT in case of major region, particularly where the GRL is not in that region. The person lead the respective regional regulatory sub-team and drive the regulatory submission in the EU region. The person ensure optimal planning in alignment with cross-functional team, and execution to plan for both development submissions and maintenance submissions to ensure ongoing compliance. Partnering with Regulatory Project Management and Submission Management is a key stakeholder management. The person participate in cross-functional and GRA initiatives.
Who you are
Considerable Regulatory Affairs experienceAdvanced scientific degree or equivalentMinimum 3 years of experience in drug development, preferably in Regulatory AffairsSkilled in matrix leadershipInfluencing and interpersonal communication skillsExcellent spoken and written EnglishDepartment: HC-RD-ROS Global Regulatory Onc Strategy
Job evaluation: AT - Expert 3
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