Senior Statistical Analyst - Programmer (Hybrid)

Senior Statistical Analyst - Programmer (Hybrid) Employer AbbVie Location North Chicago, IL Salary 96500 - 183500 USD Start date Jun 30, 2026 View more categories View less categories Discipline Information Technology , Applications/Technical Support Required Education Bachelors Degree Position Type Full time Hotbed BioMidwest , Best Places to Work Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details 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 at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The role of the Senior Statistical Analyst is to perform statistical programming activities for all assigned Phase I-IV clinical studies sponsored by AbbVie and its partners. This position performs statistical programming for clinical studies, integrated summaries, and in support of responses to requests from regulatory authorities. This position can serve as a study lead for an assigned study.

Responsibilities:

Leads the statistical programming activities, and provide programming and documentation support for multiple studies with high quality Review statistical analysis plans for all assigned studies and integrated summaries in conjunction with program lead and provide comments to study biostatistician Create ADaM data set specifications and data set for all assigned studies and integrated summaries Ensure study analysis is consistent with standard templates and specifications Contribute to submission support and support urgent regulatory agency requests Follow timelines for assigned study tasks Coordinate own task assignments Participating in a Statistical Programming process improvement initiative Manage timelines and ensure good communication with CROs/FSPs, internal programmers, statistics, data management, medical writing, regulatory publishing and clinical operations. Oversee programming tasks for a single study Conduct high level review of deliverables provided by CRO/FSP to ensure good quality and accuracy

Qualifications Minimum Qualifications:

Degree in Statistics, Mathematics, or Engineering 6+ years of relevant experience (with MS). OR8+ years of relevant experience (with BS). Experience with SAS programming related to drug development Experience with regulatory filings Experience adhering to CDISC standards and creating and reviewing ADaM speicifications

Preferred Qualifications:

Knowledge of R or Ai is not required but can be a plus.

Other Required Skills:

In-depth understanding of SAS programming concepts and techniques related to drug development. Fundamental understanding of CDISC Standards. Fundamental understanding of the drug development process. Ability to communicate clearly both oral and written. Ability to accurately estimate effort required for study related programming activities. 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 atthetimeofthis posting based on the job grade for this position.

Individualcompensation paid within this range will depend on many factors includinggeographiclocation,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 aparticular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Companys 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. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html Company 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 at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

Company info Website http:

//www.abbvie.com/ Phone 1-800-255-5162 Location 1 North Waukegan Road North Chicago Illinois 60064 United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert