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[上海]百濟(jì)神州（北京）生物科技有限公司
發(fā)布日期：2019-03-01 瀏覽次數(shù)：97
專業(yè)1:數(shù)學(xué)與應(yīng)用數(shù)學(xué)
職能類別:臨床數(shù)據(jù)分析員
2.Participates in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements.
3.Collaborates with the statistical programming staff to ensure that all programs meet analysis requirements, internal standard operating procedures, and external regulatory requirements.
4.Analyzes data and interprets results from clinical trials to meet objectives of the study protocol. Applies and implements basic and complex techniques to these analyses under supervision.
5.Prepares oral and written reports to effectively communicate results of clinical trials to the project team.
6.Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, and/or investigators.
7.Participates with management in discussions with corresponding scientific personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.8.Involved in research activities for innovative statistical methods and applications in clinical trial development
職能類別:臨床數(shù)據(jù)分析員
JD：
1.Develops individual protocols and data analysis plans and determines appropriate statistical methodology for data analysis.
2.Participates in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements.
3.Collaborates with the statistical programming staff to ensure that all programs meet analysis requirements, internal standard operating procedures, and external regulatory requirements.
4.Analyzes data and interprets results from clinical trials to meet objectives of the study protocol. Applies and implements basic and complex techniques to these analyses under supervision.
5.Prepares oral and written reports to effectively communicate results of clinical trials to the project team.
6.Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, and/or investigators.
7.Participates with management in discussions with corresponding scientific personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.8.Involved in research activities for innovative statistical methods and applications in clinical trial development
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- Requirement:
- 1.PhD or equivalent degree in statistics/biostatistics or related discipline.
- 2. Knowledge of statistical analysis methodologies and experimental design.
- 3.Working knowledge of statistical and data processing software e.g. SAS and/or R.
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