Reporting into an experienced regulatory affairs professional, you will be involved in preparing the relevant documentation for clinical trial applications in various different countries.
You will also be involved in the preparation of marketing authorisation applications and maintenance activities.
In order to be considered for this role you must be able to demonstrate the following:
· Immediately available
· Life-science degree
· Excellent attention to detail, be well-organised and able to deal with conflicting priorities
· Have previous experience in a regulatory affairs role working for global organisation
Due to the nature of the role, you will also be required to demonstrate excellent communication skills both oral and written.
Apply now for immediate consideration
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