My Basel based leading Biopharmaceutical company is seeking an exceptional CMC candidate with Excellent working knowledge/experience in regulatory submissions and approval processes for New Chemical Entities (NCE) and product life cycle management and proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements. Contact Theo Moore on +44 (0)207 801 3384 or send your CV in confidence to cv@advregualtory.com
Location: Basel - Join a leading Pharmaceutical company in a role that covers EU and Global projects. Therapeutic areas are varied and includes oncology, CNS, Immunology. You will also be working on small molecule and Biotech projects. Contact Theo Moore on+44 (0)207 801 3384 or email me at Cv@advregulatory.com
In the short-term you will take the lead for EU submissions for NME’s taking responsibility for strategy and major operational activities, before growing into a director level 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
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
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
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
This is a regulatory role for those who want to influence their own development, who are looking for a position of leadership where you have the opportunity to pursue your interests across functions and geographies.
To contact me email me Theo@advregulatory.com or call me on +44(0)207 801 3384
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.
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
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
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