Clinical Research Associate III

To ensure the rights and wellbeing of trial participants while maintaining data integrity, the full-time Clinical Research Associate III will manage site relationships, oversee clinical trial monitoring, and collaborate on regulatory submissions, working primarily in the CST/MST/PST regions. Key responsibilities Build and maintain relationships with Principal Investigators and site personnel to facilitate smooth clinical trial management Monitor investigational sites according to ICH GCP guidelines and ensure compliance with regulatory requirements Prepare site essential documents and support ethics and regulatory submissions in collaboration with the internal team Required qualifications Graduate in a clinical or life sciences-related field, with relevant experience in allied professions considered At least 2-3 years of experience as a Clinical Research Associate Experience in monitoring oncology studies Proficiency in clinical trial management systems Based in CST, MST, or PST regions