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 senior level responsibility for liaising with partners in order to facilitate the global regulatory submissions with the Health authorities and operate as a part of a small global Regulatory Affairs team providing regulatory support to operational departments - 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 is an excellent salary available for this role (up to 110,000 Euros) and this position also offers a fully expensed Car, Attractive Bonus, Shares and a Full- Re-location Package. 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
Associate Director of Regulatory Affairs is offered on a six month basis and is office based in London. One of the key objectives is to plan/manage/execute regulatory activities relating to global regulatory leadership for one or more projects. Providing regional regulatory therapeutic area strategic guidance on development projects and marketed products.
Please call 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
Senior Regulatory Affairs Associate
New Year, new budget is the mantra for many pharmaceutical companies at the moment! For this reason, a fantastic opportunity has become available with a leading CRO based in Berkshire, for a Senior Regulatory Affairs Associate. This CRO is renowned for its expertise in Clinical Trials and is therefore seeking an experienced Regulatory Affairs professional to join their EU team and work on the compilation and submission of Clinical Trial Applications.
This is great role with enough scope to keep you interested and enough development opportunities to allow you to continue to grow as a regulatory professional. 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
We are working in partnership with a fast growing pharmaceutical company based in Berkshire who is looking for a Associate Director in Regulatory Affairs. This is an excellent opportunity for an Associate Director to join the European Regulatory Affairs team in the niche area of in Orphan Drugs.
You will be a tactical / strategic thinker in the development of an existing system that logs and utilises the information from various departments including, Regulatory, Quality, Compliance and Safety from affiliates and regional HQ’s then transforming this information into Business Intelligence reports. If you wish to apply for this role send your CV to cv@advregulatory.com call Theo Moore or Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
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