Vacancy Details

CP Regulatory Affairs Consultant. Berkshire

Working for a major brand leading Pharmaceutical company that is experiencing increased workloads at the offices in Berkshire / M4 corridor, you will report to the Associate Director of European Regulatory Affairs and will be responsible primarily for an existing centralized procedure for an antiviral product. This role incorporates full product life-cycle management, as well as assisting with procedures for other products within the department as required.

This is a full-time role for at least 6 months and, although ideally it should be on site for 5 days per week, there is a possibility to be able to work from home for 1-2 days, depending on ability, experience and management discretion.

Successful applicants will have centralized procedure experience, some development (Clinical, CMC, CCDS, SmPC) experience and must be prepared to get involved in all aspects of the regulatory process, including administration.

In addition, we have another role for an Senior Clinical Development Regulatory specialist with the same client. Please call for more information.

This is an urgent position. Please contact Daniel at ProClincial on 44 (0)207 44 00 630 or email your CV with a brief description of your suitability to d.smart@proclinical.co.uk

Contract