Quotient Sciences have an exciting career opportunity at the site in Nottingham for a Regulatory Affairs Manager. In this role, you will act as Regulatory Lead in providing a centralised service coordinating regulatory submissions (CTA applications, ARSAC applications & Research Ethics Committee (REC) submissions) for clinical studies conducted by Quotient Sciences.
As the Regulatory Affairs Manager, you will drive continuous quality improvement relating to regulatory processes.
The successful candidate will be educated to a minimum degree level in a biological or life science discipline, coupled with previous regulatory experience in a similar role in a pharmaceutical company or CRO. Experience of US IND and eCTD submissions is also desirable although not essential.