继续招人~Statistical Programmer@Boston
51068
之前顺利招进一位给我投简历的朋友啦~现在组里还有一个空缺~由于简历过多抱歉不能一一回复，我会把收到的简历统一交给HR的。
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我们组现在在招人，non-profit的公司。需要近期就可以开始工作，地点波士顿，具体信息如下，有兴趣的可以把简历发至：[email protected]. 谢谢关注！
The Statistical Programmer will assist the project’s Lead Statistical Programmer with generating tables, figures, listings as outlined by the project’s biostatistician(s).
Primary Duties:
1. Program statistical analyses (i.e., tables, listings, figures, and inferential statistical output) using SAS®.
2. Act as an integral member of project team. Attend project team meetings, work with biostatisticians, data managers, and project managers.
3. Perform SAS® programming using such techniques as SAS® macro language, advanced data manipulation techniques, and statistical procedures (e.g., PROC GLM, PROC FREQ, PROC REPORT).
4. Perform quality review of SAS® programs generated by other statistical programmers and biostatisticians.
5. Review and provide feedback regarding Data Management Plans.
6. Interact with technical and clinical staff in house and with sponsors.
7. Following good programming practices and adequately documenting programs. This includes definitions that are used, individuals who provided them, and the date.
8. Be familiar with FDA regulations that affect the reporting of clinical trial data. This includes good clinical practice.
Requirements:
Education:
Master Degree in statistics, biostatistics or related field
Complexity:
Strong knowledge of SAS® programming language
Knowledge of medical and statistical terminology
Detail-oriented
Familiarity with coding dictionaries (WHO, COSTART, ICD-9, MedDRA)
Strong organizational and communication skills.
Ability to multitask and prioritize work as well as interact with project team members.
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我们组现在在招人，non-profit的公司。需要近期就可以开始工作，地点波士顿，具体信息如下，有兴趣的可以把简历发至：[email protected]. 谢谢关注！
The Statistical Programmer will assist the project’s Lead Statistical Programmer with generating tables, figures, listings as outlined by the project’s biostatistician(s).
Primary Duties:
1. Program statistical analyses (i.e., tables, listings, figures, and inferential statistical output) using SAS®.
2. Act as an integral member of project team. Attend project team meetings, work with biostatisticians, data managers, and project managers.
3. Perform SAS® programming using such techniques as SAS® macro language, advanced data manipulation techniques, and statistical procedures (e.g., PROC GLM, PROC FREQ, PROC REPORT).
4. Perform quality review of SAS® programs generated by other statistical programmers and biostatisticians.
5. Review and provide feedback regarding Data Management Plans.
6. Interact with technical and clinical staff in house and with sponsors.
7. Following good programming practices and adequately documenting programs. This includes definitions that are used, individuals who provided them, and the date.
8. Be familiar with FDA regulations that affect the reporting of clinical trial data. This includes good clinical practice.
Requirements:
Education:
Master Degree in statistics, biostatistics or related field
Complexity:
Strong knowledge of SAS® programming language
Knowledge of medical and statistical terminology
Detail-oriented
Familiarity with coding dictionaries (WHO, COSTART, ICD-9, MedDRA)
Strong organizational and communication skills.
Ability to multitask and prioritize work as well as interact with project team members.
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