My client is leading the way in the field of Health Economics, Outcomes Research, Epidemiology, Market Access, Clinical Research etc - They are looking for a talented individual to join their growing organisation. This role can be suitable to any level of candidate, from a HE analyst through to HE Director, it's really about the candidate and their background.
This organisation is able to present you with the next step in your regulatory career for those that seek cross-functional interaction as well as autonomy and career development. The therapeutic areas are varied and cover both small as well as large molecules and vaccines but full training will provided on aspect of regulatory affairs that you still need to develop. Contact Theo Moore on +44 207 801 3380 or send your Cv to Cv@advregulatory.com
Leading UK based Biopharmaceutical company is looking for a Regulatory affairs CMC Manager and Snr Manager to operate as the EU CMC product lead supporting regulatory activities for various biotechnology and chemically-derived commercial (marketed) and development (clinical) products. Contact Theo Moore +44 (0) 207 801 3384
I have a new and exciting regulatory affairs role for a Top 20 Pharmaceutical client in Brussels who is looking for a forward thinking regulatory affairs professional who would like to learn how to take the lead for EU development and Centralised MAA projects. Contact Theo Moore on +44(0)207 801 3384 or to apply email me on Theo@advregulatory.com
This 5star blue Chip Biologicals Company with an excellent pipeline and fantastic culture of innovation is expanding and developing its Global regulatory function. They now have a role available for a senior level regulatory affairs Director to take full strategic portfolio responsibility for 4-5 products in early phase development in a Global role which covers both EU and US markets. Contact Theo Moore on 0207 801 3380 or email me in confidence via Cv@advregulatory.com
This 5 Star Blue Chip Biologicals Company with an excellent pipeline and fantastic culture of innovation is expanding and developing its Global regulatory function. They now have a role available for a regulatory affairs Director to take full strategic portfolio responsibility for 4-5 products (Bio) in early phase development (from phase 1 to end of Phase 2) in a Global role which covers both EU and US markets. Contact Theo Moore 0207 801 3380 or email me in confidence to cv@advregulatory.com
My Global Pharmaceutical client based in the South-East of England is a seeking a Regulatory affairs Director for a Global Regulatory Affairs role. You will need to have in-depth knowledge and understanding of the European and regional regulatory environment and have extensive ‘hands on’ regulatory affairs experience implementing and defining regional strategy. Salary to 90K + Car and Bonus. Contact Theo Moore on +44 207 8901 3384
A top Ten Pharmaceutical client based in the South-East is seeking a Regulatory Affairs (snr) Associate for a role which will grow and develop to cover the full project lifecycle for EAME regions. Contact Theo Moore on 0207 801 3384 or send your CV in confidence to Cv@advregulatory.com
My client is a successful Brussels based Pharmaceutical Company focused on developing medicines for un-met medical needs, and continues to grow and develop at an extraordinary rate. They have ambitions to one day become a top ten pharmaceutical company and are offering fantastic opportunities to work on global development projects. Please contact Theo Moore on +44 (0)207 801 3380 or email your Cv in confidence to Theo@advregulatory.com
A dynamic and forward thinking Pharmaceutical company is looking for a Regulatory Affairs director level professional to operate as the team leader for global regulatory and EU regulatory strategies for a broad range of NCE and Biotechnology products from phase 1 through to filing. Contact Theo Moore or Matt Greig for more details on 0207 801 3384 or email theo@advregulatory.com in confidence.
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