Senior Principal Statistical Programming Lead | Equity Eligible

Biopharma Careers; San Diego (CA); On-site; USD 157,000 - 214,000; Full time

Job summary

Neurocrine Biosciences seeks a senior statistical programmer to lead major programming efforts for clinical programs. You will design, validate, and maintain SAS programs to analyze clinical data, and mentor a team of programmers across biometrics functions.

Strong leadership and vendor management are essential. Ideal candidates have extensive SAS and CDISC experience, with a track record of delivering on deadlines in a regulated biopharmaceutical environment.

Qualifications

• BS/BA degree in computer science, mathematics, statistics, or related discipline with 8+ years of statistical programming experience in biopharmaceuticals or CROs.
• Master’s or PhD with relevant experience can substitute as noted.
• Experience supervising or leading teams and managing large projects with external vendors.

Responsibilities

• Provide expert technical leadership across Biometrics and lead statistical programming efforts.
• Mentor a team of statistical programmers for clinical and nonclinical study data analyses.
• Oversee end-to-end programming work-streams across multidisciplinary programs company-wide.

Skills

SAS programming

CDISC data structures

Leadership

Project management

Communication

Analytical thinking

Regulatory knowledge

Education

BS/BA in computer science, mathematics, statistics, or related discipline

Master’s degree in computer science, mathematics, statistics, or related discipline

PhD in computer science, mathematics, statistics, or related discipline

Tools

SAS

R

CDISC standards

Job description

Neurocrine Biosciences seeks a senior statistical programmer to lead major programming efforts for clinical programs. You will design, validate, and maintain SAS programs to analyze clinical data, and mentor a team of programmers across biometrics functions.

Strong leadership and vendor management are essential. Ideal candidates have extensive SAS and CDISC experience, with a track record of delivering on deadlines in a regulated biopharmaceutical environment.