Senior Manager, Statistics

AbbVie

Confirmed live yesterday High trust

Quick summary

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

Market check

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 within the research and development organization for early oncology projects. The role involves supporting regulatory submission and product life-cycle management by providing guidance on design, analysis, and reporting for clinical trials, patient safety, and global medical affairs. Responsibilities include independently developing protocols and statistical analysis plans, identifying data collection instruments, providing programming specifications, and performing complex statistical analyses to ensure high-quality outputs. The candidate will collaborate with cross-functional teams to communicate statistical concepts clearly, manage project timelines, and lead benefit-risk planning. Required qualifications include an MS or PhD in Statistics, Biostatistics, or a related field, along with technical competence in pharmaceutical drug development and life-cycle management. The role addresses the critical challenge of advancing medicines through rigorous scientific investigation and robust data interpretation within a regulated environment.

Skills

Biostatistics Statistical Analysis Data Science Signal Detection Benefit-Risk Assessment Product Life-cycle Management Regulatory Submission Statistical Programming Safety Analysis Plans Drug Development

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, patient safety, and medical affairs.
Define programming specifications for derived variables and oversee data preparation before database lock.
Perform complex statistical analyses and evaluate the suitability of software or novel methodologies.
Create strategies for data presentation, inference, and the interpretation of statistical deliverables.
Review and ensure accuracy for scientific publications, including tables, listings, and figures.
Lead statistical support for benefit-risk planning and assessment for safety-related projects.

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 with 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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