CRA/Study Manager/CPM all for Beijing
Primary Location: China, Beijing 求人ID R0000041839 Category Clinical Trials
About this Role
CRA:
Knowledge and Experience:
• At least 1.5 years (2 years preferable) of Clinical Monitoring/ Site Management experience, global study monitoring experience is preferred
• Good knowledge of ICH/GCP, relevant international and local regulations relating to Clinical Research
Education:
• Degree in Life Science, Pharmacy, or other relevant education background
• Bachelor’s degree or above, or equivalent
Study Manager:
Knowledge and Experience:
• Minimum of BS/BA in a biomedical discipline or equivalent education/training is required.
• At least 7 years in clinical practices.
• Good working knowledge of Good Clinical Practices (GCPs), monitoring, clinical drug development process and country regulatory environment.
• Experience with clinical research methodology (e.g., study design, study monitoring and data
analysis). Prior study management and/or study coordination experience preferred.
• Demonstrated effectiveness in working in a multidisciplinary, matrix team situation.
• Advanced education and/or training/experience desirable.
Education:
• Degree in Life Science, Pharmacy, or other relevant education background
• Bachelor’s degree or above, or equivalent
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