Regulatory Affairs Manager UK&I Contract - Hays
Your new company
You will be working with a global biotechnology company located in the UK. They have quite an exciting pipeline of products across numerous therapy areas in development and on-market.
Your new role
You will be a Regulatory UK&I expert supporting both Clinical Trial Submissions and Post-marketing Maintenance. It is a varied portfolio of drugs across development and marketed products, so you will be expected to have a strong background working with the MHRA and HPRA, supporting the team with CTA's, Pips, post-licensing-maintenance.Your role will interact with global colleagues quite a bit.
What you'll need to succeed
You will need to have strong UK&I experience and experience with CTA's and post-marketing maintenance of products. Minimum of 5 years recent experience working with the MHRA and HPRA.
What you'll get in returnThis is a 12-month contract that is remote with occasional travel to site. There is a high possibility of an extension.
What you need to do nowIf you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact Julia Bowden, Recruitment Manager in Regulatory Affairs, to hear more.