Manager, Statistical Programmer at Takeda
Lexington, MA 02420
About the Job
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Noticeand Terms of Use
I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionTakeda 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 and search for Req #R0123105.LocationsLexington, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeSummaryLocation: Lexington, MAType: Full time
I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionTakeda 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 and search for Req #R0123105.LocationsLexington, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeSummaryLocation: Lexington, MAType: Full time
