Your new companyYou 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 roleYou 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 succeedYou 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.
Back to searchRegulatory Affairs Manager UK&I Contract
Hays Specialist Recruitment Limited
Posted 15 hours ago, valid for 20 days
London, Greater London EC1R 0WX
£45,000 - £54,000 per annum
Full Time
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Sonic Summary
- You will be working with a global biotechnology company located in the UK that has an exciting pipeline of products.
- The role requires a Regulatory UK&I expert to support Clinical Trial Submissions and Post-marketing Maintenance with a strong background in MHRA and HPRA.
- Candidates must have a minimum of 5 years of recent experience in these areas.
- This is a 12-month remote contract with occasional travel and a high possibility of extension.
- The salary details are not specified in the job description.
