Associate Director or Director – Global team
Permanent. Cambridge Bedfordshire Hertfordshire Suffolk Norfolk Essex Northamptonshire Leicestershire London
Are you a senior regulatory professional seeking to take the next step up in your career within Regulatory Affairs? Brand new Associate Director/Director role available in Cambridge, working in the Global team!
Senior Manager Global Regulatory Affairs CMC opportunity available on a permanent basis in Cambridge, my client is a leading Global BioPharmaceutical company with a great reputation in the market place for their innovative and ethical approach; they are also offering an excellent salary and benefits package for this highly innovative and visible role in their Global Regulatory Affairs CMC team.
Senior Manager Global Regulatory Affairs CMC opportunity available on a permanent basis in Cambridge, my client is a leading Global BioPharmaceutical company with a great reputation in the market place for their innovative and ethical approach; they are also offering an excellent salary and benefits package for this highly innovative and visible role in their Global Regulatory Affairs CMC team.
Join a leading Pharmaceutical company in a leadership role where you will be the regulatory lead for products coming through the development lifecycle. This is exciting role where you will develop regulatory strategies and work as the lead as your project goes from mid or late stage development through to filing. Contact Theo Moore or Matt Greig for more details on 0207 801 3384 or email theo@advregulatory.com in confidence.
Senior Manager / Associate Director Regulatory Affairs is required to join a growing global Biopharmaceutical company based in the South East on permanent basis. My client has an excellent product portfolio and exciting pipeline focussed on life-threatening illnesses. This role is responsible for the entirety of my clients market leading therapy portfolio and offers the successful candidate high levels of autonomy, visibility, challenge and the chance to make a difference.
Regulatory Affairs - Senior Manager Cambridgeshire 12 month contract - daily rate Non oncology TA
Due to a current vacancy, a 12 month contract has become available with one of our top clients located in Cambridge. The Regulatory Senior Manager will be working across all therapy areas except Oncology and will be working in the Global team.
This organization has an excellent pipeline and a great reputation for Oncology product development. Although this is an EU head office position there are still opportunities to grow into a Global 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
MEDICAL ADVISOR
Our client is an international pharmaceutical company with significant plans to expand their UK Medical function as part of a global restructure. This position sits as part of the UK medical affiliate reporting to the Associate Medical Director
Leading biopharma company with a first class portfolio. We are seeking an experienced Medical Advisor with industry experience to support in-line and pipeline products on around 50/50 basis. This role is in the General Medicine Group which supports Nephrology, Bone, Asthma, IBD, Diabetes, Neuroscience and Heart Failure and includes Medical Affairs and Clinical Research Phases II and III
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