Takeda Pharmaceutical Company Ltd
Manager, Statistical Programmer
Takeda Pharmaceutical Company Ltd, Lexington, Massachusetts, United States, 02173
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Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Statistical Programmer in Lexington, MA with the following requirements: Master's degree in Math, Computer Science, or related field or foreign academic equivalent plus 6 years of related experience OR Bachelor's degree in Math, Computer Science, or related field or foreign academic equivalent plus 8 years of related experience. Required skills: program analysis programs and quality control checks of analysis datasets, dataset specifications, statistical tables, figures, and listings for clinical trials; create standard macros that can be adapted to multiple studies; lead and organize study level programming and oversight activities for analysis of clinical trial data, ensuring quality and timeliness; prepare deliverables for regulatory submission to FDA/EMA/PMDA or other agencies (e.g. eCRTs, ISS, ISE, BIMO, P21 checks) and provide support for regulatory questions; perform statistical analysis using various SAS procedures such as Freq, Univariate, Means, Logistic, GLM, Mixed, and Lifetest procedures. Company headquarters in Lexington, MA. Up to 100% telecommuting allowed from any location in the U.S.
Full time $145,000.00 - $223,200 per year.
Apply on-line at https://jobs.takeda.com and search for Req #R0123105.
LocationsLexington, MA
Worker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Statistical Programmer in Lexington, MA with the following requirements: Master's degree in Math, Computer Science, or related field or foreign academic equivalent plus 6 years of related experience OR Bachelor's degree in Math, Computer Science, or related field or foreign academic equivalent plus 8 years of related experience. Required skills: program analysis programs and quality control checks of analysis datasets, dataset specifications, statistical tables, figures, and listings for clinical trials; create standard macros that can be adapted to multiple studies; lead and organize study level programming and oversight activities for analysis of clinical trial data, ensuring quality and timeliness; prepare deliverables for regulatory submission to FDA/EMA/PMDA or other agencies (e.g. eCRTs, ISS, ISE, BIMO, P21 checks) and provide support for regulatory questions; perform statistical analysis using various SAS procedures such as Freq, Univariate, Means, Logistic, GLM, Mixed, and Lifetest procedures. Company headquarters in Lexington, MA. Up to 100% telecommuting allowed from any location in the U.S.
Full time $145,000.00 - $223,200 per year.
Apply on-line at https://jobs.takeda.com and search for Req #R0123105.
LocationsLexington, MA
Worker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time