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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. Job Description
Hybrid (onsite 3 days a week / 2 days WFH / remote). Salary Range: $147,450.37 - $178,500.00 per year. Key Responsibilities
Provide expertise to design, analysis & reporting of clinical trials & scientific research studies. Independently develop protocols & statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation. Collaborate with Statistical Programming to ensure delivery of high-quality outputs according to agreed-upon timelines. Develop strategy for data presentation & inference. Work collaboratively with multifunction teams in publication of scientific research. Ensure that study results & conclusions are scientifically sound, clearly presented, & consistent with statistical analyses provided. Qualifications
PhD in Statistics, Biostatistics, Mathematics, or a highly related field & 1 year of academic, industry or research experience performing statistical data analyses. 1 Year in identifying data or analytical issues, and assisting with providing solutions. Proficiency in SAS &/or R statistical software. At least 1 pharmaceutical industry summer internship (10+ weeks) performing statistical data analyses; conducting scientific research & handling trial design, analysis & reporting of scientific research in clinical trials, inferential statistics, causal inference, or real-world analytics. Additional Information
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. 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 Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to Req ID: REF45975B
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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. Job Description
Hybrid (onsite 3 days a week / 2 days WFH / remote). Salary Range: $147,450.37 - $178,500.00 per year. Key Responsibilities
Provide expertise to design, analysis & reporting of clinical trials & scientific research studies. Independently develop protocols & statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation. Collaborate with Statistical Programming to ensure delivery of high-quality outputs according to agreed-upon timelines. Develop strategy for data presentation & inference. Work collaboratively with multifunction teams in publication of scientific research. Ensure that study results & conclusions are scientifically sound, clearly presented, & consistent with statistical analyses provided. Qualifications
PhD in Statistics, Biostatistics, Mathematics, or a highly related field & 1 year of academic, industry or research experience performing statistical data analyses. 1 Year in identifying data or analytical issues, and assisting with providing solutions. Proficiency in SAS &/or R statistical software. At least 1 pharmaceutical industry summer internship (10+ weeks) performing statistical data analyses; conducting scientific research & handling trial design, analysis & reporting of scientific research in clinical trials, inferential statistics, causal inference, or real-world analytics. Additional Information
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. 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 Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to Req ID: REF45975B
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