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Manager of Regulatory Affairs

Post updated: 24/04/2014


As a Manager of Regulatory Affairs you will manage and coordinate resources and review workload for all direct reports. You will also provide technical advice and support of clinical trials applications, regulatory requirements for study start up and clinical trials application maintenance for both internal customers and external clients. Your responsibilities will also include the preparation and coordination of global regulatory submissions to support the initiation of clinical trials for investigational drugs. You will serve as the regulatory lead on multiple projects, participate in project teams and manage specific regulatory tasks. Qualifications The successful can ...

Submission Deadline: 07/05/2014
Contact email: http://eu.experteer.com/account/signup_now/expatica_com/2587615







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