Senior Regulatory Affairs Manager Hybrid

2 weeks ago


England, United Kingdom EPM Scientific - Phaidon International Full time

We are currently seeking a talented and experienced Senior Regulatory Affairs Manager to join our client's team in Surrey. Our client is an established cosmetics/pharmaceuticals company looking for someone with expertise in global cosmetic regulations.
In collaboration with a highly skilled international team you will help to manage the clinical trial applications in Europe and other selected countries.
As the Regulatory Affairs Associate at our client's organisation, your primary responsibilities will include but not limited to:
Regulatory:
Contribute to ongoing global regulatory strategy development
Handle marketing authorisation submissions, variations, and responses to regulatory queries

Clinical trial applications:
Prepare and compile documentation for clinical trial applications in Europe and other selected countries
Manage labelling, obtain approvals, and handle amendments for clinical trials

Experience in the preparation of clinical trial applications is essential
Post-graduate qualifications in Pharmacy, Biological Sciences, or related disciplines.
Pharmaceutical industry experience
Our client offers a highly competitive salary with benefits, hybrid flexibility, impressive career progression opportunities and a chance to work alongside world-leading scientific experts.



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