Your new company

An innovative and global biotechnology company is looking to bring a Regulatory Affairs Associate II into the team for 5 months to cover maternity leave. They have a really exciting pipeline for those really driven by science.

Your new role

You will be coordinating the clinical trial submissions and notifications in the document management system and maintaining the tracking. You will be responsible for reviewing and triaging requestions for information from health authorities through CTIS to relevant teams. You will play a critical part in supporting the regulatory affairs managers with CTA submissions, having had previous experience supporting CTAs for the UK and EU.

What you'll need to succeed

Must have at least 6 months experience working with CTAs for EU markets. You must have the right to work in the UK, and be located in the UK.

What you'll get in return

Hybrid, 3 days per week for 5 months in Cambridge or Uxbridge. Good rate on offer, and a contract working for an innovative biopharmaceutical company.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV and reach out to Julia Bowden at Hays.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.