REGULATORY AFFAIRS SENIOR MANAGER | ISRAEL, RUSSIA, TURKEY | NEUROSCIENCE | RA

Your new company:
A global biopharmaceutical company with a focus in Neuroscience are looking to a Regulatory Affairs Senior Manager to work on bringing products to market within the International Growth Markets (IGM) region.

Your new role: You will be a member of the regulatory project team(s) representing Region Turkey, Israel, and Russia within the IGM.
• Your primary responsibility will be overseeing 1-3 products as they progress through the planning, filing, and approval stages of the New Drug Application (NDA) process.
• Additionally, you will ensure the availability of up-to-date regulatory documentation to support new submissions in Region these regions.
• You will provide regulatory support to the IGM regional lead for new product filings, with a specific focus on developing the NDA submission strategy and executing it these regions. As a member of the regulatory project team, you will also... contribute to the overall strategic input for the assigned product.

What you'll need to succeed:
• A minimum of 5+ years of experience in the pharmaceutical or biotechnology industry working on Israel, Turkey, or Russia regions.
• Strong skills and experience to effectively represent the Region and the IGM group on project teams.
• Experience and knowledge in preparing NDA submissions in the IGM region.

What you'll get in return:
You will have the opportunity to work with a great team expanding products into Turkey, Russia, and Israel. You will work on a 12 month contract with flexibility on site.

What to do now:
Please click "apply now" and send through an updated copy of your CV. Please reach out to Julia Bowden for any questions
United Kingdom

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