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. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. 

Key Responsibilities

• Work independently to provide statistical support to research & development org.
• Contribute to design, analysis & reporting of clinical trials or other scientific research studies.
• Act as lead statistician on clinical trial design & protocol development.
• Develop statistical analysis plans w/details for programming implementation.
• Define & implement sound statistical methodology in scientific investigations utilizing exp w/ missing data, multiple imputation & mixed effects model for repeated measures.
• Identify scientifically appropriate data collection instruments.
• Identify & report data issues or violations.
• Provide programming algorithms for derived variables & analysis datasets.

Education & Experience

Must have a PhD in Statistics, Biostatistics, Public Health, or related field & 2 years of academic or industry experience in the following:  

1. using SAS, R, & other statistical software;
2. applying &  implementing statistical methods in clinical trials;
3. performing statistical computations, simulations, and utilizing statistical methodologies for study design including sample size determination & analysis & statistical inference including   missing data imputation on various endpoints;
4. using regression analysis, multivariate analysis, design & analysis of experiments, categorical data analysis, linear models &  statistical inference including Bayesian & survival analysis in clinical trials;
5. conducting clinical trial designs, protocol development, statistical analysis plan, database activities, and scientific review & interpretation of clinical trials’ results.

Experience may be gained concurrently.

Hybrid, 3 days in office/2 days WFH.

Salary Range: $146,069.48 - $202,500.00 per year

Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to Req ID: REF45974R

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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 and long-term incentive programs.

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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