Global Regulatory Lead – Rare Disease NDA/MAA Submissions
Listed on 2026-10-04
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Pharmaceutical
Regulatory Compliance Specialist
Taylor Strategy Partners is seeking a Director/Senior Director, Regulatory Affairs to lead global regulatory strategy and submissions. The role involves ownership of major components of global submissions and agency engagement across US, EU, UK, and Japan.
Ideal candidates have 10+ years in regulatory affairs within biopharma, with proven NDA and MAA submission leadership and strong experience with EU regulatory activities for rare diseases.
The Global Regulatory Lead – Rare Disease NDA/MAA Submissions role at Taylor Strategy Partners is now open for applications in United States.
Our organisation is growing, and we are hiring a Global Regulatory Lead – Rare Disease NDA/MAA Submissions in United States.
This Full Time opening is for the Global Regulatory Lead – Rare Disease NDA/MAA Submissions role at Taylor Strategy Partners.
We are seeking a motivated Global Regulatory Lead – Rare Disease NDA/MAA Submissions to join Taylor Strategy Partners in United States.
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