European Regulatory Affairs Senior Manager- Contract
This contract is a 12 month home based role supporting a large Biotechnology company in London.
This role will provide regional regulatory support for one or more products. As a member of the Global Regulatory Team (GRT), the incumbent will be accountable for developing and executing regional regulatory strategies across the product lifecycle and managing effective agency interactions.
The individual should have a proven track record supporting the diversity of regulatory procedures in the EU (inc. CTAs, PIPs, variations, IMPDs, MAAs) and ability to work autonomously.
* Solid Regulatory Experience of 5/6 years' experience within General Medicine, someone who enjoys being a part of a Science and Innovation environment.
* Inflammation early to mid-development, Cardiovascular, Bone, therapeutic area is ideal.
* Must have good leadership and communication skills.
* Experience of working directly with the EMA and Centralised Procedure is important and must be able to work cross functionally.
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