My client is a highly successful and expanding a Bio-Pharmaceutical company with an extensive pipeline and a high value commercial portfolio who is seeking a dynamic, innovative and highly motivated personality to take the lead for EU (and sometimes Global) Regulatory strategies and submissions. This role comes with an excellent salary; full–relocation package & excellent career prospects. Contact Theo Moore on +44 (0) 207 801 3384
My client is a highly successful and expanding a Bio-Pharmaceutical company with an extensive pipeline and a high value commercial portfolio who is seeking a dynamic, innovative and highly motivated personality to take the lead for EU (and sometimes Global) Regulatory strategies and submissions. This role comes with an excellent salary; full–relocation package & excellent career prospects. Contact Theo Moore on +44 (0) 207 801 3384.
Join a global biotech organisation at their Global HQ in Switzerland where you will be offered excellent career opportunities, favorable development and the chance to lead EU or International biotech strategies and submissions.
Contact Theo Moore or Matt Greig on +44 207 801 3384 or email your CV to CV@advregulatory.com
You will be joining a great working environment with excellent benefits which are very good especially for those with children and young families. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Superb role for an accomplished Regulatory Affairs Director/Senior Director with expertise in Biologics and Biosimilars. A Biologics/Biosimilars background is essential for this role, along with Line management and an EU perspective. EU/Global Regulatory Strategy and full pipeline working knowledge. Based in the UK or France.
Superb role for an accomplished Regulatory Affairs Director/Senior Director with expertise in Biologics and Biosimilars. A Biologics/Biosimilars background is essential for this role, along with Line management and an EU perspective. EU/Global Regulatory Strategy and full pipeline working knowledge. Based in the UK or France.
Within this role you will operate as the EU and ROW regulatory partner reporting into a locally based Global Regulatory leader - If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380.
As a high performing organisation, my client is committed to growing and developing their people and within this International multi-cultural regulatory department you will find challenges and opportunities to keep you interested, motivated and developing for many years to come. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Take responsibility for a number of key projects. This high level strategic role will include providing input into the Global Regulatory Liaison for development strategy, submitting Clinical Trial Applications, project managing submission of Scientific Advice briefing packages & MAAs(or line extensions/Type II variations). Contact Theo Moore or Matt Greig on 0207 801 3384 or email CV@advregulatory.com
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