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Regulatory Affairs Associate

Post updated: 25/07/2014


As a Regulatory Affairs Associate at PRA you will work on the preparation and review of regulatory submissions for both internal customers and external clients.Responsibilities will include Preparation of clinical trial submissions to support study start up activities within PRA Tracking project timelines Supporting in the development of new processes Keeping abreast of current data, trends and developments within the global regulatory environment Qualifications To be considered for the Regulatory Affairs position you must have a BA/BSc (or equivalent) in a related science field along with some experience working within regulatory affairs ...

Submission Deadline: 07/08/2014
Contact email: http://eu.experteer.com/account/signup_now/expatica_com/2698615







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