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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..
... strategic direction of the data quality programs necessary to achieve and ... achieve and maintain high data quality in GRS systems Oversees and ... guidances with impact to BMS..
... PRINCIPAL OBJECTIVE OF POSITION Global Quality, Quality Laboratory Practices (GQ-QLP) is responsible ... preclinical research processes to determine compliance with regulatory requirements, guidelines and ... technical expertise, regulatory risk,..
... and recreational activities. Why regulatory affairs/quality assurance at Stryker? Are you ... currently seeking a Regulatory Affairs Specialist to join our Joint Replacement ... DO: As the Regulatory Affairs..
... and make a difference. The Compliance Supervisor is responsible for overseeing ... will also assist the Sr. Compliance Training Manager with Change Controls, ... Collaborates with the Manager and..