Director, Statistical Programming & Data Strategy

AbbVie; Irvine (CA); On-site; USD 180,000 - 230,000; Full time

Benefits offered by this job

Medical benefits

401(k)

Paid time off

Long-term incentives

Job summary

AbbVie in the United States seeks a Director of Statistical Programming to lead a team of programmers, aligning deliverables with the clinical development strategy across multiple indications. You will drive SAS programming excellence and ensure compliance with regulatory expectations.

The role emphasizes collaboration with cross-functional teams, SOP development, and strategic input into drug development plans while mentoring staff and advancing industry best practices.

Qualifications

• MS in Statistics, Computer Science or a related field with 12+ years of relevant experience OR BS in Statistics, Computer Science or a related field with 14+ years of relevant experience.
• Highly competent in SAS programming and Macro development.
• Pharmaceutical experience with clinical trials and regulatory filing experience (NDA/BLA, ISS/ISE).
• Minimum of 5 years of management experience and prior direct reports leadership.

Responsibilities

• Oversee a team of statistical programmers, ensuring high-quality, timely deliverables.
• Collaborate with cross-functional teams to align programming activities with clinical development strategy.
• Develop and maintain standard operating procedures to ensure regulatory compliance and industry best practices.
• Provide strategic guidance on CRFs, data standards, and analysis datasets.
• Mentor and coach junior staff, fostering a culture of scientific rigor and collaboration.

Skills

SAS Programming

Macro development

Leadership/management

Regulatory knowledge

Communication

Resource management

Education

MS in Statistics or related field

BS in Statistics or related field

Tools

SAS

Job description

AbbVie in the United States seeks a Director of Statistical Programming to lead a team of programmers, aligning deliverables with the clinical development strategy across multiple indications. You will drive SAS programming excellence and ensure compliance with regulatory expectations.

The role emphasizes collaboration with cross-functional teams, SOP development, and strategic input into drug development plans while mentoring staff and advancing industry best practices.