Regulatory Affairs Manager

Post updated: 01/09/2015

You will be responsible for managing the global submission process for assigned products of Merck Seronos General Medicines portfolio. This will include the creation and review of regulatory documents and documentation, the management of submissions to countries of the ICH regions with a main focus on Europe, Canada, Israel and Australia as well as submissions in international countries and the support of submission activities in cooperation with an external vendor. You will be member of a Regulatory Subteam and Clinical Trial Teams for assigned products and will closely cooperate with various headquarter functions and with country regulatory units of the Merck Serono organization. ...

Submission Deadline: 14/09/2015
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