Global Regulatory Submissions Project Lead
Listed on 2026-10-22
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Research/Development
Regulatory Compliance Specialist
MMS is a data-focused clinical research organization seeking a Senior Submissions Project Manager in the United States to lead IND, NDA, and MAA submissions. You will work with cross-functional teams across regulatory, clinical, biometrics, and regulatory operations to meet deadlines and ensure high-quality submissions.
You will manage budgets, timelines, risk, and client engagements, guiding teams across remote and global sites.
As a Global Regulatory Submissions Project Lead, you will play an important part at MMS in Canton Charter Township, MI, United States.
Join MMS and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Global Regulatory Submissions Project Lead role at MMS, based in Canton Charter Township, MI, United States.
We are looking to fill the Global Regulatory Submissions Project Lead position at MMS in Canton Charter Township, MI, United States.
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