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.
Responsibilities:
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
- Submit applications to competent authorities and ethics committees
- Manage labelling, obtain approvals, and handle amendments for clinical trials
- Pricing & Reimbursement:
- Handle marketing authorization applications
- Manage life cycle of approved products
Qualifications & Skills Required:
The ideal candidate should have the following qualifications/skills:
- 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.
Apply now for a chance to work for fast growing company who is directly benefiting health care and changing lives!
