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; fullâ€“relocation package & excellent career prospects. Contact Theo Moore on +44 (0) 207 801 3384
***Regulatory Affairs EU Project Manager***Switzerland***Use your CTA to Gain FULL CP Exp***Great salary & package***Top Ten Pharma still expanding*
In the first instance please call Theo Moore on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com
Associate Director Regulatory Affairs (Clinical Development)
Salary â€“ circa Â£75,000 - Â£80,000
Location - Uxbridge
Our client is actively seeking an Associate Director of Regulatory Affairs due to internal promotion within the company. This role will work across multiple therapeutic areas and is focused on Clinical and Life-Cycle Development.
Director of Regulatory Affairs & Pharmacovigilance (London)
Our client is a biopharmaceutical company that specialise in oncology products aimed at making cancer more treatable. Their mission is to acquire, develop and bring to market less toxic, more effective therapies to treat and cure cancer. Their therapeutic focus is on novel targeted therapies covering a spectrum of blood-related cancers.
Associate Director Regulatory Affairs â€“ lead early stage projects for development in the US, Europe and International â€“ FULL RELOCATION to the Netherlands ... This is a Global Regulatory Lead role graded Associate Director.
Lead early stage projects for development in the US, Europe and International â€“ FULL RELOCATION to the Netherlands ... This is a Global Regulatory Lead role graded Associate Director. If you wish to apply for this role send your CV to email@example.com or call Theo Moore on Matt Greig on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Regulatory Affairs Senior Manager *** EU Lificeycle Management functie voor een uitdagende Product Portfolio *** Nieuwe indicaties, belangrijke verlengingen *** EU en Wereldwijd Project ***
Werken als Senior Regulatory Affairs Manager betekent de verantwoordelijkheid nemen over een zeer interessante portfolio van producten.
Contacteer Matt Greig of Theo Moore op +44 (0) 207 801 3384.
Title: EU CMC RA Associate Director (Head of CMC Regulatory)
At a glance: Most senior CMC role in company, managing, EU and RoW CMC, ethical and branded.
Please call Matt Greig or Theo Moore +44 (0)207 697 7303 (eves & weekends call +44 (0)7918 679 405).
This is a highly visible role where you will lead from the front on development, strategy and agency interaction. The pipeline is exceptional you will be working from the Global Head office. Contact Theo Moore on +44(0) 207 801 3380 or email be your CV today in confidence to Cv@advregulatory.com
Mange/lead MAA submission/dossier build, with full liaison with HAâ€™s in EU for Global strategies. If you wish to apply for this role send your CV to firstname.lastname@example.org 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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