Global Regulatory Lead, Oncology & Submissions
Listed on 2026-10-11
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Pharmaceutical
Regulatory Compliance Specialist, Oncology Care
Merck’s Regulatory Affairs team in Boston seeks an Associate Director to help shape global regulatory strategy for oncology products. You will work with global leads to support registrations and lifecycle management, coordinating across clinical, CMC, and regulatory operations to drive submissions and Agency interactions.
The role emphasizes strong communication, regulatory science, and project leadership with a focus on oncology programs and continuous process improvements.
This posting is for the Global Regulatory Lead, Oncology & Submissions role at Merck, based in Boston, MA, United States.
We are currently recruiting a Global Regulatory Lead, Oncology & Submissions for our team in Boston, MA, United States.
This is a genuine opening to take on the Global Regulatory Lead, Oncology & Submissions role at Merck.
As a Global Regulatory Lead, Oncology & Submissions, you will play an important part at Merck in Boston, MA, United States.
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