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Job description
Parexel seeks a Senior Clinical Research Associate (Sr. CRA) to lead site management, monitoring, and close-out for assigned trials, ensuring patient safety and quality in line with GCP and sponsor standards.
Responsibilities include site activation through database lock, acting as primary site contact, and coordinating with the SCP. Travel 60–80% to support investigator sites and ensure enrollment and data integrity.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.