A top Ten Pharmaceutical client based in the South-East is seeking a Regulatory Affairs (snr) Associate for a role which will grow and develop to cover the full project lifecycle for EAME regions. Contact Theo Moore on 0207 801 3384 or send your CV in confidence to Cv@advregulatory.com
Join an organisation that has excellent training and development opportunities and interesting and commercially focused EU regulatory projects. The product range is varied and the scope for developing your experience and expertise is excellent. Please Contact Theo Moore on +44 (0)207 801 3384 or email your CV in confidence to CV@advregualtgory.com
*** Regulatory Affairs CMC Marketed Products Switzerland - Join a first rate Pharma Company with an outstanding regulatory environment!
Please call one of Advanced Regulatory's principals for Regulatory Affairs, Marc Van de Voorde or or Theo Moore on +41 (0) 41 710 51 00 or +44 (0)207 801 3382. Alternatively you can email us on cv@advregulatory.com
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
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
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
Join a leading pharmaceutical company with a fantastic pipeline, offering great projects, full project autonomy, fantastic promotion prospects, and the opportunity to grow into a Global RA Director - 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
Join a Blue-chip Pharma company in Global role with a great salary, exceptional relocation package and a highly rated pipeline. 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 successful Brussels based Pharmaceutical Company focused on developing medicines for un-met medical needs, and continues to grow and develop at an extraordinary rate. They have ambitions to one day become a top ten pharmaceutical company and are offering fantastic opportunities to work on global development projects. Please contact Theo Moore on +44 (0)207 801 3380 or email your Cv in confidence to Theo@advregulatory.com