Senior Regulatory Affairs Consultant

STR Health

Job Description

My client is a leading global Clinical Research Organisation providing clinical development solutions to biopharmaceutical companies. The organisation now has an exciting vacany for a Senior Regulatory Affairs Consultant in their office in Scotland. You will be a regulatory affairs professional with substantial regulatory affairs experience and probably come from a clinical trials environment or CRO background. You will provide a high level of technical expertise to external clients and inhouse associates. The post might suit a very experienced Regulatory Affairs Officer wanting to step up as well as a seasoned Consultant. You will have proven expertise in managing submissions including IND, NDA, MAA. and CTD. You will also need to be degree educated in a life science or relevant science subject, probably with a second, higher degree. A committed regulatory affairs professional, you will be a member of TOPRA. The post is permanent, full-time and offers remuneration in the range of £30-35,000, depending on experience. Please email your CV and supporting information to jshipman@strgroup.co.uk or phone John Shipman on 02392 314674 for details.