Strategic Leader, Statistical Programming

Allergan; North Chicago (IL); On-site; USD 150,000 - 210,000; Full time

Job summary

AbbVie in the United States is seeking a Manager of Statistical Programming to guide a team of statistical programmers in early development, interfacing with Statistics, Data Sciences, Medical Writing and Regulatory Publishing.

The role requires leading SAS programming for ADaM datasets and Tables, Listings and Figures, with strong CDISC knowledge, and the ability to partner with cross-functional teams on regulatory submissions.

Qualifications

• MS or BS with 8+ / 10+ years of experience in statistical programming.
• Experience leading a team of statistical programmers.
• Strong knowledge of SAS concepts and CDISC standards.
• Experience with regulatory filings and drug development.
• Excellent communication and cross-functional collaboration skills.
• Ability to estimate effort for programming activities.

Responsibilities

• Leads statistical programming activities for early development programs.
• Manages a team of statistical programmers and resource planning.
• Ensures timely deliverables and maintains quality processes.
• Develops SAS programs for ADaM datasets and tables/listings/figures.
• Creates documentation for regulatory filings.
• Mentors junior staff and interfaces with cross-functional teams.

Skills

Team leadership

SAS programming

CDISC standards

Drug development

Regulatory filings

Cross-functional collaboration

Communication skills

Education

MS in Statistics, Computer Science or related field

BS in Statistics, Computer Science or related field

Tools

SAS software

Job description

AbbVie in the United States is seeking a Manager of Statistical Programming to guide a team of statistical programmers in early development, interfacing with Statistics, Data Sciences, Medical Writing and Regulatory Publishing.

The role requires leading SAS programming for ADaM datasets and Tables, Listings and Figures, with strong CDISC knowledge, and the ability to partner with cross-functional teams on regulatory submissions.