The Site Management Lead (SML) is a key member of the Clinical Study Team (CST), responsible for overseeing all site management and monitoring activities conducted by the Contract Research Organization (CRO) in a clinical study. SML ensures high-quality execution of site-related processes from site selection through to site closure, while maintaining compliance with regulatory standards and study protocols. SML collaborates closely with Clinical Trial Lead (CTL), CST and the CRO to develop study-specific operational plans, including the Clinical Monitoring Plan, and plays a critical role in identifying and mitigating study-level risks.

Responsibilities: