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... Myers Squibb Clinical Trial Result Specialist in Princeton New Jersey Bristol-Myers ... The Clinical Trial Results Reporting Specialist is responsible for creation of ... the databases. The Results Reporting..
... Research and Development / Global Regulatory, Safety and Biometrics / Global ... and Biometrics / Global Submissions Regulatory Policy - Global Regulatory Business Capabilities Functional Area Description ... Capabilities..
... PRINCIPAL OBJECTIVE OF POSITION Global Quality, Quality Laboratory Practices (GQ-QLP) is responsible ... preclinical research processes to determine compliance with regulatory requirements, guidelines and established standard ... an emphasis..
... and make a difference. The Compliance Supervisor is responsible for overseeing ... will also assist the Sr. Compliance Training Manager with Change Controls, ... of training programs that meet..
