BioSpace
Pharmacometrics Analyst (SAS Programming)
BioSpace - North Chicago, Illinois, us, 60086
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Overview
Pharmacometrics Analyst (SAS Programming)
Join to apply for the
Pharmacometrics Analyst (SAS Programming)
role at
BioSpace . Position located in North Chicago, IL, with a salary range of $110,500.00-$199,000.00. Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address future medical challenges. We aim to impact people's lives across immunology, oncology, neuroscience, eye care, and aesthetics. For more information, visit
www.abbvie.com . Job Description
The Statistical Analyst plays a key role in pharmaceutical research and development, focusing on analysis and reporting of clinical trial data. Responsibilities include developing SAS programs for data sets, tables, listings, and figures, validating data, and creating documentation for regulatory submissions. Responsibilities
Lead statistical programming activities for routine studies. Develop SAS programs following CDISC standards for ADaM data sets, tables, listings, and figures. Validate data sets and reports. Create specifications and documentation for regulatory filings. Participate in the development of standard SAS macros. Qualifications
MS in Statistics, Computer Science, or related field with 3+ years of experience, or BS with 5+ years. Practical knowledge of SAS programming related to drug development. Basic understanding of CDISC standards and drug development process. Excellent communication skills. Additional Information
This position requires onsite presence 3 days/week. Compensation varies based on location and experience, with benefits including health insurance, paid time off, and 401(k). AbbVie is an equal opportunity employer.
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Join to apply for the
Pharmacometrics Analyst (SAS Programming)
role at
BioSpace . Position located in North Chicago, IL, with a salary range of $110,500.00-$199,000.00. Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address future medical challenges. We aim to impact people's lives across immunology, oncology, neuroscience, eye care, and aesthetics. For more information, visit
www.abbvie.com . Job Description
The Statistical Analyst plays a key role in pharmaceutical research and development, focusing on analysis and reporting of clinical trial data. Responsibilities include developing SAS programs for data sets, tables, listings, and figures, validating data, and creating documentation for regulatory submissions. Responsibilities
Lead statistical programming activities for routine studies. Develop SAS programs following CDISC standards for ADaM data sets, tables, listings, and figures. Validate data sets and reports. Create specifications and documentation for regulatory filings. Participate in the development of standard SAS macros. Qualifications
MS in Statistics, Computer Science, or related field with 3+ years of experience, or BS with 5+ years. Practical knowledge of SAS programming related to drug development. Basic understanding of CDISC standards and drug development process. Excellent communication skills. Additional Information
This position requires onsite presence 3 days/week. Compensation varies based on location and experience, with benefits including health insurance, paid time off, and 401(k). AbbVie is an equal opportunity employer.
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