Senior Manager, Statistics

AbbVie

Confirmed live yesterday High trust

Quick summary

Work type: On-site
Location: Chicago, IL
Salary: $124,500–$236,500 / yr
Posted: 6 days ago
Freshness: Confirmed live yesterday
Closes: Sep 29, 2126
Nearby: 99+ roles within 25 mi

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Salary context

Competitive pay

How this pay compares to similar roles

Similar $187k

This role $180k

$111k most similar roles pay here $250k

This role pays more than 56% of similar roles. Most pay $159,000–$214,900 — the shaded band above. At the midpoint, this role pays about $180k versus about $187k for comparable roles.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 261 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 241 roles with salary data.

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At a glance

TL;DR · Senior Manager, Statistics

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Senior Manager, Statistics provides statistical leadership for the research and development organization to support early oncology projects. This role involves managing clinical trials, patient safety, and global medical affairs by developing protocols, statistical analysis plans, and data collection instruments. The individual will perform statistical analyses, provide programming specifications for derived variables, and ensure the accuracy of data released for analysis. Key responsibilities include designing research programs, evaluating software for planned analyses, and collaborating with cross-functional teams to communicate complex concepts to non-statisticians. Candidates must possess an MS or PhD in Statistics or Biostatistics and demonstrate technical competence in drug development and life-cycle management within a regulated environment. The role addresses the critical challenge of advancing medicines through rigorous scientific investigation, benefit-risk assessment, signal detection, and the preparation of high-quality reports for regulatory submissions.

Skills

Biostatistics Statistical Analysis Data Science Signal Detection Benefit-Risk Assessment Drug Development Product Life-cycle Management Statistical Programming Data Collection Instruments

What you'll do

Provide statistical leadership for the design, analysis, and reporting of clinical research programs and regulatory submissions.
Develop protocols and statistical analysis plans for clinical trials, product safety, and medical affairs evidence generation.
Define programming specifications for derived variables and oversee data preparation before database lock.
Perform complex statistical analyses and evaluate the appropriateness of software or novel methodologies for scientific investigations.
Create strategies for data presentation, inference, and the accurate interpretation of results in reports and publications.
Lead statistical support for benefit-risk planning and assessment to address both pre-planned and ad hoc safety requests.
Communicate complex statistical concepts clearly to non-statistical stakeholders across cross-functional teams.

What we're looking for

MS with 8+ years of experience or PhD with 4+ years of experience in Statistics, Biostatistics, or a related field.
High degree of technical competence and effective oral and written communication skills.
Ability to manage project timelines and ensure the quality of deliverables.
Strong leadership skills and experience managing cross-cultural or overseas teams.
Oncology experience (preferred).
Pharmaceutical or related industry knowledge including drug development and life-cycle management in a regulated environment (desired).
Experience supporting safety-related projects such as ISS, benefit-risk assessment, or signal detection (preferred).

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