Regulatory Submissions Lead - MLR & Client Ops
RAPP San Francisco
RAPP is seeking a Regulatory Operations Specialist to support the MRM Health regulatory submissions for the Princeton client base. You will lead day‑to‑day submissions, coordinate with cross‑functional teams, and manage submission workflows from kickoff to final Client MLR approval. The role requires 2–4 years of related experience, familiarity with FDA guidelines, strong writing and communication skills, and proficiency with MS Office and regulatory systems such as Veeva Vault. #J-18808-Ljbffr RAPP
Vacancy posted 1 day ago
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