Senior Statistical Programming Manager - Remote

Takeda Pharmaceutical Co.

Cambridge (MA)

À distance

USD 116 000 - 182 000

Plein temps

Il y a 43 heures
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Avantages offerts par ce poste

Medical benefits
401(k)
Paid time off
Holidays

Résumé du poste

Takeda Development Center Americas, Inc. in Cambridge, MA seeks a Manager, Programming to lead study-level statistical programming and oversight.

Plan, drive, and deliver analysis datasets, tables, listings, figures, and submission-ready deliverables, coordinating with Statistics, Data Management, and Clinical Operations teams. The role requires expertise in CDISC standards, SAS and R, and experience with regulatory submissions (ISS/ISE).

Qualifications

  • Master's degree or Bachelor's degree in Statistics, Mathematics, Biostatistics, Computer Science, Data Science, Business Analytics, or related field with 4+ years (Master's) or 6+ years (Bachelor's) of related experience.
  • Experience developing SDTM/ADaM datasets per CDISC standards for regulatory submissions.
  • Experience with SAS procedures (FREQ, UNIVARIATE, MEANS, LOGISTIC, GLM, MIXED, LIFETEST) and regulatory deliverables.

Responsabilités

  • Lead end-to-end statistical programming activities for clinical trials.
  • Develop and review analysis datasets, TLFs, ISS/ISE, and submission deliverables.
  • Ensure CDISC standards, data quality, and regulatory timelines.

Connaissances

Leadership
Project management
Communication

Formation

Master's or Bachelor's in Statistics/Mathematics/Biostatistics/CS/Data Science/Business Analytics or related field

Outils

SAS
R
CDISC
Regulatory submissions

Description du poste

Takeda Development Center Americas, Inc. in Cambridge, MA seeks a Manager, Programming to lead study-level statistical programming and oversight.

Plan, drive, and deliver analysis datasets, tables, listings, figures, and submission-ready deliverables, coordinating with Statistics, Data Management, and Clinical Operations teams. The role requires expertise in CDISC standards, SAS and R, and experience with regulatory submissions (ISS/ISE).

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