Manager, Statistical Programming (Oncology)

Allergan; Greenlawn (NY); Remote; USD 160,000 - 197,000; Full time

Job summary

Join a forward-thinking company that is dedicated to discovering innovative medicines. As a key player in the statistical programming team, you will lead the development of vital pharma products, ensuring compliance with industry standards. Your expertise in SAS programming and CDISC standards will be crucial in shaping the future of healthcare. This role offers the flexibility of 100% telecommuting, allowing you to thrive in a supportive environment while making a meaningful impact on patients' lives. If you are passionate about data and its role in transforming healthcare, this opportunity is perfect for you.

Benefits

Paid Time Off

Medical/Dental/Vision Insurance

401(k)

Short-term and Long-term Incentive Programs

Qualifications

• 5+ years of statistical programming experience, especially with SAS.
• Experience with CDISC standards and regulatory filings.

Responsibilities

• Guide a team of statistical programmers in drug development.
• Develop SAS programs for creating ADaM datasets.

Skills

SAS Programming

Statistical Analysis

CDISC Standards

Data Analysis

Team Leadership

Education

Bachelor's in Statistics

Master's in Statistics

Tools

SAS

ADaM

SDTM

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 and research & develop new pharma products.
• Lead programming for a compound/indication or therapeutic area in early and/or late-stage development, interfacing with Statistics, Data Sciences, Medical Writing, Regulatory Publishing & Clinical Operations.
• Develop and oversee the development of Statistical Analysis System (SAS) programs for creating 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, and 5 years of statistical programming experience. The experience must include: (i) 5 years utilizing SAS programming concepts and techniques related to drug development and regulatory filings; (ii) 5 years applying CDISC standards, including ADaM and Study Data Tabulation Model (SDTM); (iii) 5 years developing SAS programs for creating ADaM data sets following CDISC standards, and for generating Tables, Listings, & Figures; (iv) 3 years working in a matrixed organization across stakeholders and functions to gather, analyze, synthesize requirements, and translate them; (v) 2 years developing standard SAS macros; (vi) 1 year providing oversight and mentoring of assigned Statistical Programmers & Analysts. Alternatively, a Master’s degree in Statistics, Computer Science, or a related field with 2 years of statistical programming experience is acceptable. The experience must include: 2 years with (i)-(iii); 1 year with (iv) & (v); and 6 months with (vi).

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

100% telecommuting is allowed.

Additional Information

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

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

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

AbbVie is an equal opportunity employer committed to operating with integrity, driving innovation, transforming lives, and serving our community. We are an Equal Opportunity Employer/Veterans/Disabled.

For US & Puerto Rico applicants, to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation can learn more here: https://www.abbvie.com/join-us/reasonable-accommodations.html