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Regulatory Affairs

Senior RA Specialist needed for 16 hours per week on an initial 3 month hourly rate contract. The role can be based remotely with 1 or 2 site visits per month to the client who is based in Dublin

As the Senior Regulatory Affairs Consultant you will be responsible for medicinal product strategy, preparing and maintaining the company's product registrations (for existing products and under development) for designated territories.

This is an initial 3 month contract covering 16 hours per week. The role will be mostly based remotely and site visits would be 1 or 2 days a month.

Day-day duties:

-Create and execute Regulatory Strategies related to existing and new MAA's.

-Preparing and submitted of new MAA's across multiple territories (primarily EU) using DCP

-Preparing and managing international regulatory submissions in accordance with commercialisation plan.

-Renewing and updating product certificates/ in company's territories -

Providing regulatory support for out-licensing activities in EU and non-EU territories

If you are interested in this role please apply below or get in touch for immediate review.

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

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales