Company: Advanced Regulatory (EU Roles)
Location: Europe, Belgium, Brussels
Closing Date: 18 Jul 15
Type: Full Time
Salary (£): 100,000+
Benefits: FULL RELOCATION * FANTASTIC SALARY AVAILABLE * APPLY TODAY FOR MORE INFORMATION *
OPTION Belgium * * * Global Regulatory Leader for major biotechnology company *** Beat the downturn, low tax rate and high salaries plus relocation There are three good reasons to consider this opportunity are in the advert, please click to read more. To apply for this position please contact me, Matt Greig or Theo Moore on +44(0)207 801 3384 or by email to Theo@advregulatory.com also I can be contact out of working hours seven days a week on +44 (0) 7918 195 166
OPTION Belgium * * * Global Regulatory Leader for major biotechnology company *** Beat the downturn, high salaries plus relocation
Location: Europe, Belgium,
In the first instance please call Matt or Theo on+44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com
Title: OPTION Belgium * * * Global Regulatory Leader for major biotechnology company *** Beat the downturn, high salaries plus relocation
There are three good reasons to consider this opportunity:-
1.The role is global with own project and product responsibilities, you will mentor EU and US partners in this role in a company with the strongest portfolio we know of.
2.Gain further US FDA liaison and lead US, EU and Japanese partners, this role will prime you for much more senior positions.
3.Low tax rate, you can rent out your mortgaged home out and with the pound this weak, send money back to the UK at an excellent rate if it is temporarily unlet. Rentals for large flats are extremely low compared to the UK and South East.
We have two positions for Associate Director / Director level individuals with a well-known organisation. These are roles “close to the filing and indications” rather than dedicated line management ones. You are the most senior Regulatory lead on your drug development project and you will lead and direct by matrix regulatory teams in the US, EU and Japan.
Most individuals in this role have two to three MAA filings in a major region (US or EU) and want to consolidate and gain Global strategy rather than just be an EU or US regulatory expert. You will be responsible for early stage and late stage compounds, mostly biotechnology but not always, from fist time in man to preparation to file and approval. You will look after Target Product Profiles, Product Evaluation Portfolios, master planning, PoC, preparation for 2a and 2b meetings as well as full leadership of regulatory liaisons for filings.
You will have 8-10 years in EU or US regulatory affairs at a Senior Manager or Associate Director level, and want to play your part at the highest level. PhD is preferential but not a prerequisite.
About Advanced Regulatory
Many people tell us our adverts & communication makes sense. Why work with an agency which does not know the difference between RoW and an RMS? We provide a high level of service because we work with Regulatory people every day and we know our subject matter.
To apply for this position please contact me, Matt Greig or Theo Moore on +44(0)207 801 3384 or +44 (0) 7918 195 166 or by email to Theo@advregulatory.com also I can be contact out of working hours seven days a week on +44 (0) 7918 195 166
Keywords / Key words: Regulatory Switzerland, Regulatory Strategy, Regulatory Affairs Basel, Regulatory Affairs, Regulatory Affairs Switzerland, Regulatory Affairs, Regulatory, Regulatory Affairs, Regulatory, Regulatory Affairs, RA, Regs, Clinical Development, Project Manager, Centralised Procedures, MAA MRP, CHMP, Rapporteur, CTA, Ethical, NCE, NBE, Pharmaceutical, Biotech.
1 Calico House
Clove Hitch Quay
|Tel:||+44 (0)207 801 3380|
|Website:||Visit Our Web Site|
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.