Senior Regulatory Affairs Manager
12 Month Contract
Based in London or Cambridgeshire
Offering up to 60 Per Hour
We are working with a Global biotech company that are seeking an experienced individual to support multiple oncology products from a European regulatory perspective. Successful applicants will have strong experience in submissions and licensing ensuring licenses are acquired and maintained in order to support clinical trials for investigational medicinal products.
Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals. Understanding of drug development Scientific / Technical Excellence
Comprehensive understanding of regulatory activities, touch points and how they affect projects and processes
Excellent communication skills
Must be able to live and work in the UK.
If this position is of interest to yourself, please send your CV to email@example.com
- Agency: Clinical Professionals
- Contact: Ben Loader
- Reference: JO-2006-451081_2
- Updated: 22nd June 2020
- Expires: 20th July 2020