Senior Clinical Research Associate, APAC

Purpose Statement:

Monitors progress of clinical studies at the site level to verify that the rights and well being of subjects are protected, that the reported study data are accurate, complete, and verifiable from source documents, and that the study is conducted in accordance with protocol, standard operating procedures, ISO/GCP and other applicable regulatory requirements. Provides support in start up, enrollment, follow up and closure of clinical trial activities. 

The role of Senior Clinical Research Associate as a Lead Monitor is responsible for the compliance and oversight of clinical trials that implement a Risk-Based Monitoring (RBM) strategy and being the main point of contact between the study team and site monitors. The role includes performing study compliance oversight by conducting Site Compliance Meetings, analyzing data to identify potential compliance outliers, and working with study teams and sites to resolve identified issues. The lead...