Regulatory Affairs Contractor

An exciting new role for a six month interim period for a leading Pharmaceutical organisation. The role will be initially based 5 days a week in their Surrey head office however there is flexibility for home working after an initial period. It is essential that the candidate must have EU or UK and Ireland experience regulatory experience. The purpose of the role will be to manage and maintain product marketing aurthorisations and clinical trial aurthorisations. You will be working in the Worldwide regulatory strategy team. The ideal candidate will need to have the following experience and expertise: - Managing and submitting marketing aurthorisations - National/MRP/Decentralised MAA - Manage and submit MA variation applications - Interaction with regulatory aurthorities - Clinical trial approvals - Expeirence working with Medicinal products A suitable candidate will also have strong written and communication skills along with proven strength in analytical thinking. My client will be looking to have initial interviews arranged for next week so if this role is of interest to you then please don't hesitate to contact Peter Duvall at Real Staffing on 02077587367

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com/uk