Regulatory Affairs
Project Manager, Biotech A regulatory affairs professional with the ability to
project manage is being sought by my client. This position offers an attractive remuneration package and is with a company rated very highly by other regulatory professionals in the industry. The purpose of this role includes the co-ordination of the preparation, assessment and submission to European regulatory authorities, such as pre-meeting packages, scientific advice, orphan drug designation applications, clinical trial applications and marketing applications. In this role you will be handling products in development, clinical trials and those which are already marketed. Ideally you will have working knowledge within these areas as well as a scientific background in genetics and some experience in medical devices. Do apply immediately if you are interested and for more information call Mark OHalloran ...
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