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Regulatory Consultant Netherlands

Regulatory Consultant - Netherlands 6 month contract

I am currently looking for an experienced Regulatory consultant for a 6 month contract in the Netherlands working for a large Pharmaceutical / Biotec company.
The client is a market leader and is highly sought after client in the Pharmaceutical environment.
You will need to have at least 6 years experience within regulatory affairs and have a decent knowledge of the European legislation, centralized procedure and EU clinical Trial Directive.
Your skill set must include project management, Fluent in English both written and oral and be experienced with the Microsoft office.
The role will be based on the client site just outside Amsterdam and you will be working on site directly with the EMEA director. The role will be working on full lifecycle projects looking at the management of these and working on submissions and variations. Type I, Type II variations, PSUR ASP and PIP. You must also have knowledge of CTA and be able to competently tackle questions related to these to ensure accuracy.
Please send me your CV or call me on the direct number below and I will be happy to talk over the Regulatory Affairs positions that I have further with you.

My dd is +442392322389 and my e-mail is rkelly@strgroup.co.uk so please get in touch.




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