Senior Clinical Research Coordinator - Protocol & Study Lead
Tulane group
Tulane University is seeking a Clinical Research Coordinator III to coordinate all aspects of a clinical study with minimal supervision. The role requires in-depth protocol knowledge and GMP practices to support investigators and maintain regulatory files. The position involves screen/enroll of participants, data collection, and noninvasive testing, while serving as a primary resource for protocol and liaison among patients, investigators, and IRB teams, ensuring compliance and quality across #J-18808-Ljbffr Tulane group
Vacancy posted 16 hours ago
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