Lead Statistical Programming Manager (SAS/CDISC)

Allergan; South San Francisco (CA); On-site; USD 180,000 - 240,000; Full time

Job summary

AbbVie in South San Francisco is seeking a Manager of Statistical Programming to lead a team of programmers in the early development of new medicines. You will interface with Statistics, Data Sciences, Medical Writing and Regulatory to guide programming efforts and ensure high-quality deliverables.

The role emphasizes SAS programming, ADaM data sets, CDISC standards, and mentoring staff to support regulatory filings and cross-functional collaboration.

Qualifications

• MS in Statistics, Computer Science or a related field with 8+ years of relevant experience.
• BS in Statistics, Computer Science or a related field with 10+ years of relevant experience.
• Previous 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.

Responsibilities

• Leads the statistical programming activities for a compound/indication or therapeutic area in early development.
• Leads a team of statistical programmers and manages the resource planning for assigned staff.
• 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 participates in the development of standard operating procedures.
• Provides oversight and mentoring of assigned Statistical Programmers, Statistical Analysts and Senior Statistical Analysts.

Skills

Team leadership

SAS programming

CDISC standards

Drug development

Communication skills

Education

MS in Statistics/CS or related field

BS in Statistics/CS or related field

Tools

SAS

SAS Macros

CDISC standards

Job description

AbbVie in South San Francisco is seeking a Manager of Statistical Programming to lead a team of programmers in the early development of new medicines. You will interface with Statistics, Data Sciences, Medical Writing and Regulatory to guide programming efforts and ensure high-quality deliverables.

The role emphasizes SAS programming, ADaM data sets, CDISC standards, and mentoring staff to support regulatory filings and cross-functional collaboration.