Global Rassu Regulatory Lead

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Skills

GCP

Description

Please submit your application in English

What You'll Do

The Global RASSU Lead will serve as a subject matter expert for clinical trial regulatory

requirements

, ensuring alignment with country-specific

requirements

, CTI and sponsor SOPs, ICH/GCP, and applicable regulations.

The role will also support regulatory document oversight, study start-up tracking, eTMF/TMF review, audit readiness, training and mentoring, and communication with sponsors and cross-functional teams.Global and Regional Reg…

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