Statistical Programmer (Hybrid)

ABBVIE; North Chicago (IL); On-site; USD 66,000 - 126,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie is seeking a Statistical Programmer to join our R&D team. You will analyze and report clinical trial data under the direction of a Senior Statistical Analyst and interface with Statistics, Clinical Data Strategy & Operations, Medical Writing, Regulatory Publishing and Development Operations.

The role emphasizes SAS programs for ADaM data sets following CDISC, development of Tables, Listings and Figures, and creation of regulatory data documentation.

Qualifications

• Ability to communicate clearly both oral and written.
• MS or BS with relevant field and experience.
• Demonstrated practical understanding of SAS programming and PK analysis.

Responsibilities

• Create documentation for regulatory filings including reviewers guides and data definition documents.
• Develop SAS macros and data processing processes for analysis-ready datasets.
• Consolidate heterogeneous data sources to prepare analysis-ready data sets for studies.
• Perform exploratory data analyses and visualizations in collaboration with pharmacometricians.
• Produce dynamic and static data visualizations to communicate quantitative analyses.

Skills

Communication

Education

MS in Statistics/CS

BS in Statistics/CS

Tools

SAS

ADaM

Job description

• Compensation: USD 65500 - USD 125500 - yearly

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com . Follow @abbvie onLinkedIn, Facebook ,Instagram ,X andYouTube.

Job Description

The Statistical Programmer is an integral project team member in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data under the direction and oversight of a Senior Statistical Analyst. The Statistical Programmer interfaces with key stakeholders (i.e. Statistics, Clinical Data Strategy & Operations, Medical Writing, Regulatory Publishing and Development Operations.)

Responsibilities

• The Statistical Programmer will:
  • Create documentation for regulatory filings including reviewers guides and data definition documents.
  • Participate in the development of standard SAS Macros.
• The Programmer will:
  • Consolidate heterogeneous data sources (e.g. clinical study databases, external databases, real-world data) to prepare analysis-ready data sets within a defined quality control process supporting a particular study.
  • Perform exploratory data analyses and visualizations in interaction with the clinical pharmacologist or pharmacometrician.
  • Produce dynamic and static data visualizations to communicate quantitative analyses.
• - Develop SAS programs for the creation of ADaM data sets following CDISC standards
• - Develop SAS programs for the creation of Tables, Listings and Figures.
  • Validation of ADaM data sets.
  • Validation of Tables, Listings and Figures.
  • Create specifications for the structure of ADaM data sets for individual studies.

Qualifications

Minimum Qualifications

• MS in Statistics, Computer Science or a related field with 0+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 2+ years of relevant experience.
• Demonstrated practical understanding of SAS programming and experience with pharmacokinetic (PK) analysis and reporting.
• Ability to communicate clearly both oral and written.

Preferred Qualifications

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law.

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

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