Clinical Trial Associate: Start-Up & Regulatory Documentation

Novartis Singapore is seeking a Clinical Trial Associate (CTA) to support the Study Start-up Manager and Clinical Research Associate throughout the study lifecycle. Responsibilities include managing document preparation for IRB submissions and ensuring compliance with regulatory requirements. The ideal candidate will have a degree in a scientific or medical field with prior experience in clinical operations, along with a basic understanding of ICH/GCP and regulatory guidelines. J-18808-Ljbffr