Description
This leading pharmaceutical company is looking for a Regulatory Professional for a six month contract based from their office in the South East.
The right candidate would have worked in a similar position previously and have experience of:
1. European Regulatory Procedures and experience of Centralised Procedure would be an advantage.
2. Clinical trial procedures across the EU and the EU clinical trial directive.
3. Post approval support of marketed products (variations, line extensions).
Know of post approval and life cycle management as well as interacting with Regulatory agencies would be an advantage
The purpose of the role is to allow the client to legally study, manufacture market and supply medicines. To obtain, mange and maintain productMarketing Authorisation and Clinical Trial Authorisation in line with business goals and legal requirements. Under the guidance and supervision of Regulatory Affairs Managers, to conduct associated regulatory activities for theUK and Irish markets and contribute to Departmental projects.
To Apply to this position, pls contact Graham Everitton and/or send your details.