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AbbVie
Senior Statistical Analyst - Programming - Oncology (Hybrid)
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What they do
A Statistician collects and analyzes data using the principles of statistics, for work in science, psychology, politics, marketing and manufacturing. Analyzes data and makes policy recommendations to government agencies that address economic, environmental and public health issues.
$106,122 / year median in California
+2% projected growth
Job Description
Company DescriptionAbout AbbVieAbbVie'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 DescriptionThe Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.
Leads the statistical programming activities for studies.
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, Tables, Listings and Figures.
Create specifications for the structure of ADaM data sets for individual studies and integrated data.
Create documentation for regulatory filings including reviewers guides and data definition documentsLeads the development of standard SAS Macros and participates in the development of standard operating procedures.
Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.
Fundamental understanding of CDISC Standards.
Fundamental understanding of the drug development process, including experience with regulatory filings.
Ability to communicate clearly both oral and written.
Ability to accurately estimate effort required for study related programming activities.
Additional InformationApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.
Job DescriptionThe Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.
Responsibilities:
Leads the statistical programming activities for projects with lower complexity.Leads the statistical programming activities for studies.
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, Tables, Listings and Figures.
Create specifications for the structure of ADaM data sets for individual studies and integrated data.
Create documentation for regulatory filings including reviewers guides and data definition documentsLeads the development of standard SAS Macros and participates in the development of standard operating procedures.
Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.
QualificationsMinimum Qualifications:
Bachelors in Statistics, Computer Science or a related field8+ years of relevant experience in quantitative analysis (or 6+ with a Masters)Experience with SAS ProgrammingExperience leading programming for clinical trialsPreferred Qualifications:
Masters Degree in Statistics, Computer Science or related fieldR Programming experienceOncology specific experienceOther Required Skills:
Indepth understanding of SAS programming concepts and techniques related to drug development.Fundamental understanding of CDISC Standards.
Fundamental understanding of the drug development process, including experience with regulatory filings.
Ability to communicate clearly both oral and written.
Ability to accurately estimate effort required for study related programming activities.
Additional InformationApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.