drjobs Sr. Manager Statistical Programmer

Sr. Manager Statistical Programmer

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1 Vacancy
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Job Location drjobs

Boston - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Responsibilities:
  • The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products.
  • The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area.
  • This role must effectively interface with Statistics Data Sciences Medical Writing Regulatory Publishing and Development Operations.
  • Leads the statistical programming activities for one or more compounds/indications or a therapeutic area.
  • Manages a team of statistical programmers and the resource planning for their assigned projects.
  • Ensures timely deliverables that all quality processes are followed and consistency within the projects.
  • Develops and oversees the development of SAS programs for the creation of ADaM data sets following CDISC standards.
  • Develops and oversees the development of SAS programs for the creation of Tables Listings and Figures.
  • Ensures consistency of ADaM data sets for individual studies and integrated data.
  • Creates documentation for regulatory filings including reviewers guides and data definition documents.
  • Leads the development of standard SAS Macros and the development of standard operating procedures.
  • Manages mentors and creates career development plans for assigned staff.
  • Participates in the recruitment and selection of new staff.
Requirements:
  • MS in Statistics Computer Science or a related field with 9 years of relevant experience.
  • OR BS in Statistics Computer Science or a related field with 11 years of relevant experience.
  • Minimum of 2 years experience leading a team of statistical programmers.
  • In-depth understanding of SAS programming concepts and techniques related to drug development.
  • In-depth understanding of CDISC Standards.
  • In-depth understanding of the drug development process including experience with regulatory filings.
  • Ability to communicate clearly both oral and written.
  • Ability to effectively represent the Statistical Programming Organization in cross functional teams.
  • Ability to accurately estimate effort required for project related programming activities.

Employment Type

Full Time

Company Industry

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