Manager, Statistical Programming (Oncology)

AbbVie Inc; North Chicago (IL); Remote; USD 160,000 - 197,000; Full time

Job summary

An established industry player is seeking a skilled statistical programmer to lead innovative projects in pharmaceutical research. This role involves guiding a team through the development of new products while ensuring adherence to industry standards. Candidates should have a strong background in SAS programming and statistical analysis. With 100% telecommuting permitted, this position offers flexibility and the chance to make a significant impact on health solutions. Join a forward-thinking company committed to excellence and community service, and enjoy a comprehensive benefits package.

Benefits

Paid Time Off

Insurance

401(k)

Incentive Programs

Qualifications

• 5 years of experience in statistical programming and drug development.
• Expertise in SAS programming and CDISC standards.

Responsibilities

• Guide a team of statistical programmers in R&D of new pharmaceutical products.
• Lead programming efforts for specific compounds in development.

Skills

SAS Programming

Statistical Analysis

CDISC Standards

Data Management

Education

Bachelor's in Statistics

Master's in Statistics

Tools

SAS

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Key Responsibilities

1. Guide a team of statistical programmers in research and development of new pharmaceutical products.
2. Lead programming efforts for a specific compound, indication, or therapeutic area in early and/or late-stage development, interfacing with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Clinical Operations.
3. Develop and oversee the creation of Statistical Analysis System (SAS) programs for Analysis Data Model (ADaM) data sets following Clinical Data Interchange Standards Consortium (CDISC) standards.

Education & Experience

Must have a BS in Statistics, Computer Science, or a related field, with 5 years of statistical programming experience. The required experience includes: (i) 5 years utilizing SAS programming concepts related to drug development and regulatory filings; (ii) 5 years applying CDISC standards, including ADaM and SDTM; (iii) 5 years developing SAS programs for ADaM data sets following CDISC standards and for Tables, Listings, and Figures; (iv) 3 years working in a matrixed organization across stakeholders; (v) 2 years developing standard SAS macros; (vi) 1 year providing oversight and mentoring of statistical programmers and analysts. Alternatively, a Master’s degree with 2 years of relevant experience is acceptable, with similar specific experience requirements.

Experience can be gained concurrently. Any combination of education and work experience is acceptable.

100% telecommuting is permitted.

Additional Information

Salary Range: $160,000 - $197,000 per year.

Apply online at https://careers.abbvie.com/en. Refer to Req ID: REF39459F.

We offer a comprehensive benefits package including paid time off, insurance, and 401(k). This position is eligible for incentive programs.

AbbVie is an equal opportunity employer committed to integrity, innovation, and community service. For more information, visit here. Applicants seeking accommodations can learn more at this link.