发布日期: |
2008-08-14 | 招聘人数: |
1人 | 工作地点: |
上海市 | 职位性质: |
全职 |
工作经验: |
一年以上 | 学历要求: |
博士 | 语言能力: |
英语一般 | 职位月薪: |
面议 |
年龄要求: |
不限 | 身高要求: |
不限 | 性别: |
不限 | ||
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| -Design, Analyze, and Interpret Clinical Trials -Provide statistical expertise and contributions for projects and protocols in support of PGRD Clinical development. -Provide statistical expertise on regulatory submissions and ensure quality and appropriateness of submission deliverables. -Provide statistical expertise to maximizing the value of aggregate clinical data in support of scientific and drug development strategies. -Provide study level statistical leadership and communicate resource needs to CPW and CSDM leads. Requirements: -Advanced degree in statistics, biostatistics, or related field -Capability to provide statistical leadership to cross -functional teams at the protocol level. -Strong statistical skills with application to clinical trials. -Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization. -Relevant clinical trial and business experience providing an understanding of the processes associated with clinical, regulatory and marketing operations. -Prior experience varies with career ladder level from D2 (MSc and 0 years) |
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