Job Details

Job Summary:

This is great time to join a Pharmaceutical company with a great reputation for innovation and a pipeline that cover small and large molecule projects. As the Global Regulatory Liaison you will have the final say for all regulatory matters on your projects and products in Global markets. This is a great next step for those who want REAL GLOBAL RESPONSIBILITY. Contact Theo Moore on +44 207 801 3384

Requirements:

Regulatory Affairs Global Liaison Role –EU and US markets – Expanding Pharma with great potential –

Location: Brussels, Belgium

My client is looking for a candidate with at least At least 10 years relevant experience in the pharmaceutical industry and a road background of experience working in one, possibly more areas in regulatory affairs, e.g. Global, US, European, International, CMC or at Health Authority. You will have excellent experience in successfully contributing to delivering competitive regional regulatory approvals and proven leadership and program management experience.

My client has a number of Global filings planed for it’s expansive product range over the next 4 years and this role will allow you to be part of the HQ RA function which may allow more strategic RA activities in a global environment. You will also be tasked with helping to contribute to shape the RA Department with further opportunities for coaching and people development. Within this position (which comes with both Direct reports in Brussels, and Matrix reporting in the US) options to further grow and progress vertically at mid term will definitely be available.

With regards to Agency interactions you are the last say in RA strategy for your projects and the fulfilment of these strategies.. you are the top level..!!!

______________________________________

TO APPLY:
If you wish to apply for this role please send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Theo Moore or Matt Greig on 0207 801 3384

About ADV Regulatory
Advanced Regulatory has operating since 2004. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs, Quality Assurance, Clinical Development, Pharmacovigilance and Health Economics and Outcomes Research. We match professional candidates to the best permanent, contract and interim roles in the market.
Visit us at www.advregulatory.com

Key words: Regulatory, Regulatory Affairs, Reg Affairs, Regulatory Affairs Director, Regulatory Affairs Associate Director, Regulatory Affairs Senior Manager, Regulatory Affairs Manager, Regulatory Affairs Executive, Regulatory Affairs Officer.