Senior Regulatory Affairs Lead, Global Submissions
Listed on 2026-10-20
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Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
Nuvation Bio, Inc. is seeking an experienced Regulatory Affairs professional to lead regulatory strategies and manage submissions for development programs in oncology.
You will work with cross-functional teams and global partners to plan, prepare, submit, and maintain INDs, NDAs, DMFs, and CTAs, while ensuring compliance with FDA regulations. The role requires at least 10 years in regulatory affairs, familiarity with eCTD and e-publishing, and strong communication skills.
The Senior Regulatory Affairs Lead, Global Submissions role at Nuvation Bio, Inc. is now open for applications in Boston, MA, United States.
We are currently recruiting a Senior Regulatory Affairs Lead, Global Submissions for our team in Boston, MA, United States.
This is a genuine opening to take on the Senior Regulatory Affairs Lead, Global Submissions role at Nuvation Bio, Inc.
As a Senior Regulatory Affairs Lead, Global Submissions, you will play an important part at Nuvation Bio, Inc. in Boston, MA, United States.
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