【Statistical Programmer Position at Boston】# JobHunting - 待字闺中
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The Statistical Programmer will assist project’s lead statistical
programmer on 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:
MS/MA or equivalent in statistics, biostatistics, or related field;
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.
If you have interests, please send your resume to v*************[email protected]
programmer on 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:
MS/MA or equivalent in statistics, biostatistics, or related field;
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.
If you have interests, please send your resume to v*************[email protected]
