职责描述：
Skills
• Good computer skills including but not limited to the knowledge of Clinical Trial/PV Systems/Data Management Systems, MS-Office products such as Excel, Word
• Preferred experience/expertise in clinical practice beyond training with a strong medical/scientific knowledge, and/or experience with case/medical review
• Demonstrate a sound awareness of all relevant regulations, including GCP, GVP, etc.
• Good knowledge of SOPs/Working Instructions /System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as E2A, E2B and E2D, and proven practical application
• Ability to successfully work in a (‘virtual’) team environment
• Client focused approach to work
• Knowledge of medical terminology and awareness of coding dictionaries (e.g. MedDRA & WHODRUG)
• Solid interpersonal, verbal and written communication skills
• Sense of urgency in completing assigned tasks
• Meticulous attention to detail
• Independently motivated, detail oriented and strong problem-solving ability
• Effective time management in order to meet daily metrics or team objectives
• Shows commitment to and performs consistently high quality work
Education
• Bachelor or above degree with medical qualification or relevant medical experience
Language Skills
• Competent in written and oral English.
Minimum Work Experience Three years PV Physician working experience for a Master’s degree candidate is required.
任职要求：
具体请参见药品安全医生JD

其他信息
语言要求：英语