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Job description
Bristol Myers Squibb is seeking a Clinical Research Associate to oversee site monitoring, data integrity, and regulatory compliance across trial sites in the San Antonio / South-Central Texas region. Travel up to 70% may be required, with responsibility for site qualification, initiation, routine monitoring and close-out visits per ICH GCP and SOPs.
The role emphasizes collaboration with internal teams, vendor sites, and investigators to ensure patient safety and trial integrity, while
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Worksite address
houston, TX, 77246, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.