Manager, Statistical Programming (Oncology)

Agnello & Rogers; North Chicago (IL); Remote; USD 160,000 - 197,000; Full time

Job summary

A leading company in pharmaceuticals is seeking a Statistical Programmer to guide a team in the development of new products. The role involves programming efforts in drug development, requiring a strong background in SAS and CDISC standards. This position allows for 100% telecommuting and offers a competitive salary along with a comprehensive benefits package.

Benefits

Comprehensive benefits package

Paid time off

Medical/dental/vision insurance

401(k)

Short-term and long-term incentive programs

Qualifications

• 5 years of statistical programming experience, including SAS and CDISC.
• Experience in drug development and regulatory filings.
• 1 year providing oversight and mentoring to programmers.

Responsibilities

• Guide a team of statistical programmers in R&D of pharmaceutical products.
• Lead programming efforts for compounds in development.
• Develop SAS programs for Analysis Data Model datasets.

Skills

SAS programming

CDISC standards

Statistical analysis

Team leadership

Mentoring

Education

BS in Statistics, Computer Science, or related field

Master’s degree in related field

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.

Job Description

Key Responsibilities

• Guide a team of statistical programmers in research and development of new pharmaceutical products.
• Lead programming efforts for a compound, indication, or therapeutic area in early and/or late-stage development, interfacing with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Clinical Operations.
• 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.

Qualifications

Education & Experience

Must have a BS in Statistics, Computer Science, or a related field, with 5 years of statistical programming experience. Specifically, experience should include: (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 and for Tables, Listings, and Figures; (iv) 3 years working in a matrixed organization across stakeholders and functions; (v) 2 years developing standard SAS macros; (vi) 1 year providing oversight and mentoring to statistical programmers and analysts. Alternatively, a Master’s degree in a related field with 2 years of relevant experience is acceptable, with corresponding experience in (i) through (iii), (iv) & (v), and 6 months in (vi).

Experience may be gained concurrently. Any suitable combination of education and work experience will be accepted.

This position allows for 100% telecommuting.

Additional Information

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

Apply online at https://careers.abbvie.com/en, referencing Req ID: REF39459F.

We offer a comprehensive benefits package including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k). This role is eligible for short-term and long-term incentive programs.

AbbVie is an equal opportunity employer committed to integrity, innovation, transforming lives, and serving our community. We welcome applications from Veterans and Disabled individuals.

For US & Puerto Rico applicants seeking accommodations, please visit: https://www.abbvie.com/join-us/reasonable-accommodations.html