This is a one year contract for an experienced Regulatory Affairs Manager based or willing to commute to Cambridge. This role will support one or more products from a regional regulatory perspective. As a member of the Global Regulatory Team , you will achieve the desired labelling by developing and executing regional regulatory strategies and managing effective agency interactions. Limited Company Contractors only.
Operate as a Regulatory Affairs Manager in role which is based around providing strategic leadership for MAA’s, lifecycle and development for products in the EMEA region for Oncology Biotech projects - 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
Opportunity for an experienced Emerging Market Regulatory Affairs Manager to join this global Pharma Company on a permanent basis. Remit includes line managing 2 Senior Regulatory Associates, ensuring effective strategic input to Global Regulatory Plans, and that teams / functional groups are provided with clear, constructive regulatory input to assist planning and issue resolution across lifecycle activity. Excellent promotional / development opportunities.
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
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
This is great role for a company on the move. They have successfully grown their pipeline into what is widely recognized as one of the best in the industry for a company of this size. You will be working in an expansive role, covering early and late stage development projects, Centralised filings and lifecycle management of the company’s most successful products. Contact Theo Moore on 0207 801 3384 or email your CV in confidence to cv@advregulatory.com
This is an exciting opportunity to take control of a growing EU Regulatory department and set up the relevant systems and processes to help the company deliver success as it continues to grow. Contact Theo Moore or Matt Greig on 0207 801 3380 or email us today via cv@advregulatory.com
I have a new and exciting regulatory affairs role for a Top 20 Pharmaceutical client in Brussels who is looking for a forward thinking regulatory affairs professional who would like to learn how to take the lead for EU development and Centralised MAA projects. Contact Theo Moore on +44(0)207 801 3384 or to apply email me on Theo@advregulatory.com
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