Abbott
Strategic Statistical Analyst – Abbott
Abbott is a global healthcare leader with a portfolio that spans diagnostics, medical devices, nutritionals, and branded generic medicines. We are seeking a Strategic Statistical Analyst to join our team in Chicago, IL.
Key Responsibilities
Work with project teams to determine appropriate study design and statistical/data‑science methodology.
Conduct comprehensive protocol reviews, randomization schedules, sample‑size and power calculations.
Ensure data accuracy for statistical analyses.
Implement protocol methodology and statistical analysis plans.
Deliver accurate and timely statistical input into reports or decisions.
Validate alternative analysis strategies when changes to planned analyses are needed.
Create computer programs that are accurate, efficient, and well documented.
Demonstrate extensive understanding of statistical concepts and methodologies.
Compare and evaluate the real‑life value of products and therapies with clinical trial and epidemiology data.
Scientific Reports and Publications
Authorship of Statistical and Data‑Science Methods sections of protocols and peer‑reviewed literature.
Ensure accuracy of statistical tables, data listings, and report text.
Identify and correct flaws in interpretation of results, inconsistencies in presentation, or inference.
Provide significant and timely input to the development of a report strategy.
Consultation
Collaboratively develop efficient designs, quality protocols, and reports per agreed timelines.
Provide accurate and timely answers to routine and non‑standard questions from clients.
Maintain good client relationships and develop strategies for expanding the client base.
Communicate an understanding of product development and act in accordance with those principles.
Effectively present statistical concepts and arguments to management, regulatory agencies, and scientists.
Contribute to the development of a clinical program strategy.
Training, Mentorship, & Supervision
Mentor less‑experienced statisticians.
Lead a team of statisticians and programmers on clinical trials.
Provide formal training to statisticians and non‑statisticians.
Serve as a project leader on key initiatives.
Project Coordination & Regulatory Activities
Coordinate and lead the section’s work across multiple projects to ensure regulatory compliance.
Interact with project leaders and regulatory affairs.
Ensure accurate and appropriate statistical input for regulatory submissions, discovery, and development decisions.
Design, plan, and execute analytical components of intellectual property submissions, peer‑reviewed literature, clinical trials, and data‑collection activities.
Ensure consistency and accuracy between report text and statistical tables.
Identify and correct common flaws in interpretation of results and adherence to Abbott report guidelines.
Provide meaningful input to the development of a report strategy.
Communicate basic statistical concepts to scientists and non‑scientists.
Qualifications
Bachelor’s Degree.
Minimum 4 years of relevant experience.
Preferred Qualifications
Programming experience in SAS or R.
Experience with clinical trials analysis, and coursework or experience with data‑science techniques.
Strong communication and presentation skills.
Experience with publications, health economics and outcomes research (HEOR), and patent applications.
Location & Compensation Chicago, IL – $75,300 – $150,700 per year.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Industries Hospitals & Health Care
Abbott is an Equal Opportunity Employer, committed to employee diversity.
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Key Responsibilities
Work with project teams to determine appropriate study design and statistical/data‑science methodology.
Conduct comprehensive protocol reviews, randomization schedules, sample‑size and power calculations.
Ensure data accuracy for statistical analyses.
Implement protocol methodology and statistical analysis plans.
Deliver accurate and timely statistical input into reports or decisions.
Validate alternative analysis strategies when changes to planned analyses are needed.
Create computer programs that are accurate, efficient, and well documented.
Demonstrate extensive understanding of statistical concepts and methodologies.
Compare and evaluate the real‑life value of products and therapies with clinical trial and epidemiology data.
Scientific Reports and Publications
Authorship of Statistical and Data‑Science Methods sections of protocols and peer‑reviewed literature.
Ensure accuracy of statistical tables, data listings, and report text.
Identify and correct flaws in interpretation of results, inconsistencies in presentation, or inference.
Provide significant and timely input to the development of a report strategy.
Consultation
Collaboratively develop efficient designs, quality protocols, and reports per agreed timelines.
Provide accurate and timely answers to routine and non‑standard questions from clients.
Maintain good client relationships and develop strategies for expanding the client base.
Communicate an understanding of product development and act in accordance with those principles.
Effectively present statistical concepts and arguments to management, regulatory agencies, and scientists.
Contribute to the development of a clinical program strategy.
Training, Mentorship, & Supervision
Mentor less‑experienced statisticians.
Lead a team of statisticians and programmers on clinical trials.
Provide formal training to statisticians and non‑statisticians.
Serve as a project leader on key initiatives.
Project Coordination & Regulatory Activities
Coordinate and lead the section’s work across multiple projects to ensure regulatory compliance.
Interact with project leaders and regulatory affairs.
Ensure accurate and appropriate statistical input for regulatory submissions, discovery, and development decisions.
Design, plan, and execute analytical components of intellectual property submissions, peer‑reviewed literature, clinical trials, and data‑collection activities.
Ensure consistency and accuracy between report text and statistical tables.
Identify and correct common flaws in interpretation of results and adherence to Abbott report guidelines.
Provide meaningful input to the development of a report strategy.
Communicate basic statistical concepts to scientists and non‑scientists.
Qualifications
Bachelor’s Degree.
Minimum 4 years of relevant experience.
Preferred Qualifications
Programming experience in SAS or R.
Experience with clinical trials analysis, and coursework or experience with data‑science techniques.
Strong communication and presentation skills.
Experience with publications, health economics and outcomes research (HEOR), and patent applications.
Location & Compensation Chicago, IL – $75,300 – $150,700 per year.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Industries Hospitals & Health Care
Abbott is an Equal Opportunity Employer, committed to employee diversity.
#J-18808-Ljbffr