This role could be for 6 or 12 months (your choice) and you will be joining a well-run and friendly team in role with lots of autonomy and strategic input - My client is also happy to wait for a 1 month notice. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
There are currently opportunities to work on products in all stages of development (phases 1,2 and 3) for small and large molecule products in roles that encourage regulatory y leadership, RA strategy, agency negotiation and leading Centralised MAA’s. Contact Theo Moore on +44 207 801 3380 or email me your CV via CV@advregulatory.com
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
Operate as the Global Regulatory Lead and/or EU Regulatory Lead on a global Life Cycle Team or Marketed Product Team for complex and/or business critical projects for a leading Bio-Pharmaceutical based in Switzerland. This role comes with a strong team and strong portfolio of both Pharma and Biological products. Contact Theo Moore on +44 (0)207 801 3384
Please call me, Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com
Regulatory Affairs (Snr) Manager - International/Row role – Switzerland. This is a newly created vacancy with the aim of developing this candidate into an Associate director with people and project management responsibility. Join one of the world’s leading companies in a proactive and exciting roll. In the first instance please call Theo Moore or Matt Greig on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Cv@advregulatory.com
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
Learn how to provide leadership for regulatory submissions whilst providing strategic and innovative thinking for major pharms and biotech projects/submissions (for EU and/or International territories) - 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
If you have over 7 years Regulatory CMC experience for development and MAA activities and are looking for a great next challenge, then this could be the role for you… In the short term you will be leading CMC regulatory teams to develop global CMC regulatory strategy...In the long term you will grow to lead and manage your own team whilst gaining biotech experience. Call Theo Moore or Matt Greig on +44 (0)207 801 3380 or email your CV to CV@advregulatory.com
This company is highly rated within the industry and is well on it’s way to becoming the worlds No.1 Pharmaceutical Company. The pipeline is rich and diverse, and includes Pharma and Biotech compounds. For this role you will operate as the EU Regulatory liaison for Oncology. 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
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