
Senior Clinical Research Associate - Texas - FSP
Senior CRA accountable for site activation, monitoring, issue resolution and close-out of investigator sites to ensure patient safety and trial quality per GCP and sponsor standards. Requires minimum 3 years' site monitoring experience (preferably 2 years in oncology), a life sciences degree or equivalent, fluency in English, and ability to travel 60–80% (valid driver’s license and passport required).








