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[담당업무] 1.Projects/Clinical Studies
• Participate in project meetings and client meetings as Subject Matter Expert for Clinical Data Management (CDM) providing advice on all aspects of CDM processes, systems and tools in view of client's business objectives, regulatory requirements and Novotech best practices.
2.Team
• Participate in industry forums (conferences, professional association committee work etc.) and providing training on CDM related topics to Biometrics and wider Novotech organisation.
3.Software Tools
• Monitor and advise Line Manager on new capabilities of EDC platforms and related clinical trial applications from a CDM perspective by participating in online user forums and attending workshops/ meetings/conferences as appropriate.
4.CDM Processes and SOPs
• Lead the development and updating of SOPs and best practices, process improvement, quality control and governance related to all CDM matters.
[근무부서 및 직급/직책]
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[자격요건] 경력사항: 경력(8년 이상 )
학력사항: 대학교(4년)졸업
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