Senior Manager, Statistical Programming – Drug Development

ABBVIE

Irvine (CA)

On-site

USD 110,000 - 209,000

Full time

35 hours ago
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Job summary

AbbVie is seeking a Manager of Statistical Programming in Irvine, CA to lead a team of statisti cal programmers in early development efforts. You will oversee SAS programming for ADaM data sets, Tables, Listings and Figures, align with CDISC standards, and partner withStatistics, Data Sciences, Medical Writing and Regulatory teams.

You will mentor staff, manage resource planning, and ensure timely, compliant deliverables.

Qualifications

  • MS in Statistics, Computer Science or related field with 8+ years of relevant experience or BS+10+ years
  • Experience leading a team of statistical programmers
  • Deep SAS programming knowledge for drug development and CDISC standards

Responsibilities

  • Leads the statistical programming activities for a compound/indication or therapeutic area in early development.
  • Leads a team of statistical programmers and manages resource planning for assigned staff.
  • Ensures timely deliverables and adherence to quality processes across projects.
  • Develops and oversees SAS programs for ADaM data sets and Tables, Listings and Figures.
  • Ensures consistency of ADaM data sets across studies and integrated data.
  • Creates regulatory documentation including reviewers guides and data definition documents.
  • Leads development of standard SAS Macros and SOPs.
  • Provides oversight and mentoring of assigned programmers and analysts.

Skills

Leadership
Communication
Cross-functional collaboration
Project management
Analytical thinking

Education

MS in Statistics or related field
BS in Statistics or related field

Tools

SAS programming
CDISC Standards
ADaM data sets
SAS Macros

Job description

AbbVie is seeking a Manager of Statistical Programming in Irvine, CA to lead a team of statisti cal programmers in early development efforts. You will oversee SAS programming for ADaM data sets, Tables, Listings and Figures, align with CDISC standards, and partner withStatistics, Data Sciences, Medical Writing and Regulatory teams.

You will mentor staff, manage resource planning, and ensure timely, compliant deliverables.

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