Forward thinking client which is rated in the Top 10 of world Pharmaceutical companies - Excellent Benefits package which includes a great salary & benefits package - Strong pipeline with Oncology, CNS, Pain, Inflammation and Cardiovascular products in late phases of development - Location: Switzerland, Basel, Neuchâtel, Geneva,
In the first instance please call Matt or Theo on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@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
I am currently working with a Global Pharma to develop a new Oncology and Pain Regulatory team. This Global branded Pharmaceutical Company has recently been through an acquisition in Europe. As a result they are building a new team in their EU Headquarters which is based in the UK.
Therefore I am looking for 5 individuals who are keen to be involved in these exciting and rare opportunities. Please find some brief details below.
This organisation has a healthy pipeline of early and late stage development projects and the regulatory department is uniquely set-up in such a way that you will have full project responsibility and leadership for your own Centralised registrations. 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
This is a great opportunity to join a company which has shown an excellent levels of growth and has a promising future - 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 regulatory affairs role covering Europe (EU and non-EU countries), Asia Pacific, Latin America, Middle East, Russia and CIS countries, North America and Africa. Cover projects at different stages of drug development ranging from products in clinical development (Phases I to IV) to approved products. Excellent salary, bonus and re-location available. Contact theo Moore or Matt Greig on +44 207 801 3380
Regulatory Project Manager – UK/Ireland/Malta team
Permanent / Bedfordshire
Are you a regulatory professional seeking to take the next step up in your career within Regulatory Affairs? Brand new Regulatory Project Manager role available in Bedfordshire, working in the UK team!
Regulatory Affairs Manager - Germany
Baden-Wurttemberg, Office-based. An exciting opportunity has arisen for an experienced Regulatory Affairs Manager looking for a new, diverse challenge in Regulatory Affairs. My client, a global pharmaceutical company is looking for a Manger to provide leadership to a team of associates and consultants, provide a variety of consulting services, and to work within project guidelines to achieve project objectives and address client issues.
Regulatory Affairs Manager - Switzerland
Basel or Geneva, office-based. An exciting opportunity has arisen for an experienced Regulatory Affairs Manager looking for a new, diverse challenge in Regulatory Affairs. My client, a global pharmaceutical company is looking for a Manger to provide leadership to a team of associates and consultants, provide a variety of consulting services, and to work within project guidelines to achieve project objectives and address client issues.
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