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Parexel is seeking a Clinical Research Associate to support clinical trial delivery for assigned investigator sites. The role oversees site monitoring from activation through database lock, ensures regulatory and protocol compliance, manages site issues and safety reporting, and collaborates with study teams to achieve quality and timeline objectives. Responsibilities Ensure proper conduct of clinical trials in accor

Responsibilities Develops strong site relationships and ensures continuity of site relationships through all phases of the trial Performs clinical study site management/monitoring activities in compliance with International Conference on Harmonization / Good Clinical Practices, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated Documents Gains an in-depth understanding of the study