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The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.

The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials, ensuring compliance with regulations and quality standards, and enhancing investigator site relationships.

The Senior Clinical Trial Manager oversees operational aspects of clinical trials from start-up to database lock, ensuring compliance with GCP and SOPs, managing vendors, and coordinating trial activities and communications with stakeholders.