Senior Regulatory Affairs Manager - Clinical Trial

We are currently seeking a talented and experienced Senior Regulatory Affairs Manager to join our client's team. 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!