2024-07-11

高级临床数据经理(外派外资药厂)(J21300)面议

上海市 | 若干人

职位描述:

• Clinical Research Team
• Quality Assurance / Quality Control
• Local drug supply chain
• R&D, GMA, Global ESRO, etc
• Procurement
• Regulatory Affairs
• Principal Investigator/Co-Investigators
• Results Driven Behavior
• Self-motivation and adaptability
• History of successful managerial experience on project management
• Ability to form strong alliances with marketing teams and among own team members
Technical / skill training / 技 术 / 技 能 训 练
• Data Management Experience
• Knowledge of GCP, SOPs and drug development and regulations
• Comprehensive knowledge of CDASH/SDTM/ADaM CDISC standards and metadata management
Skills for CRF/eCRF design
• Cross-function experience in drug development, particularly CRF/eCRF design and DM
• Ability to see cross-project dependencies and act to resolve issues
• Good presentation and communication skills across different business areas ( Internal , External)
• Effective meeting and

任职资格:

• Well-developed communication, organizational, and interpersonal skills
• Ability to adapt learning and development models
• Highly developed consultative skills
• Negotiation skills
• Results driven, customer service orientation

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