As Senior Regulatory Affairs Associate, responsibility will be covering lifecycle activity within the EU, Emerging and African regions for a blockbuster product and other specialist therapy areas. Including; the preparation, submission and review of CTAs, MAAs, IMPD, PIPs. This role will suit a candidate with relevant experience looking for an organisation to develop within.
Regulatory Affairs Associate Director. Therapeutically focused in Oncology. Permanent
Are you a senior Regulatory professional seeking to take the next step up in your Regulatory Affairs Career? If so, I have a fantastic permanent Regulatory Associate Director role available with a leading global pharmaceutical/R&D company located in London!
This is a great opportunity to join an expanding Biotech company with an excellent pipeline and a good number of recent MAA successes. Your role will be to take Regulatory responsibility for the development and leadership of the regulatory strategy for an exciting early stage (PI & PII) portfolio of biological products. Contact Theo Moore on+ 44 (0)207 801 3380 or email me in confidence via email@example.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 companyâ€™s most successful products. Contact Theo Moore on 0207 801 3384 or email your CV in confidence to firstname.lastname@example.org
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 email@example.com in confidence.
Our client is a Global leader and pioneer in the Biotechnology field using innovative research to drive the discovery and development of important therapeutics. This top company has a strong development pipeline with strong prospects in Oncology, Osteoporosis and Renal. They are currently seeking a Senior Regulatory Labelling Associate for a 12 month contract based in Cambridgeshire.
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 firstname.lastname@example.org 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
My blue chip Pharmaceutical client is now looking to expand their EMEA Regulatory affairs team and are now searching for a number of experienced, motivated and talented individuals for a number of Regulatory roles based at their European Head office. Contact Theo Moore on +44 207 801 3380
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her