via Career pages·4d ago
Clinical Research Associate II
Fortrea
Full-timeOn-siteclinical site managementich gcp complianceclinical monitoringsite initiationprocess monitoringdata integrity verificationeclinical systemsclinical trial management systemsource document reviewquery generationadverse event reportingstakeholder managementiso 14155medical device knowledgepharmacologyanalytical skillsproject planningtraining delivery
Location:BANGALORE, Karnātaka, IndiaType:Full-timePosted:4d ago
Summary of Responsibilities. Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requi...
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