Submission. Specialist in CTA preparation activities for initial filings and start up activities, protocol amendments, end... compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance...
Bristol-Myers SquibbSubmission. Specialist in CTA preparation activities for initial filings and start up activities, protocol amendments, end... compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance...
Bristol-Myers Squibb(First In Human) studies within the EMEA. Experience of the regulatory and site start up requirements for clinical sites..., from start-up to close-out. Advanced knowledge of study management best practices and tools and has shown...
Gilead