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Regulatory Submissions Specialist — Clinical Trials

Medpace | singapore, Singapore | Posted June 10, 2026

Position Overview

A leading clinical research organization in Singapore is seeking a full-time Regulatory Submissions Coordinator. This role supports clinical trials by managing regulatory submissions and ensuring compliance with regulations. Candidates should have a relevant bachelor's degree and 2 years of experience in a CRO or pharmaceutical company. The position offers a flexible work environment and competitive compensation, along with various career advancement opportunities.
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