Responsibilities

The Senior Clinical Research Associate will monitor assigned clinical trials in China to ensure data integrity and adherence to regulations, company policies, and applicable procedures, serving as the primary point of contact with site staff. They will verify study conduct, ensure reporting of adverse events, verify data accuracy, conduct monitoring visits, prepare study materials, and communicate relevant information to project managers. Additionally, the role involves maintaining expertise in China regulations, participating in investigator meetings, generating status reports, tracking regulatory documents, and addressing noncompliance issues at investigative sites.