Manager, Statistics, Oncology

AbbVie

Confirmed live yesterday High trust

Hybrid

Quick summary

Work type: Hybrid
Location: Florham Park, NJ
Salary: $109,500–$208,500 / yr
Posted: 2 days ago
Freshness: Confirmed live yesterday
Closes: Oct 8, 2126
Nearby: 99+ roles within 25 mi

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $169k

This role $159k

$98k $220k

below market most similar roles pay here above market

This role pays less than 58% of similar roles. Most pay $140,000–$198,000 — the blue band above. At the midpoint, this role pays about $159k versus about $169k 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 156 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 146 roles with salary data.

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At a glance

TL;DR · Manager, Statistics, Oncology

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The Manager, Statistics - Oncology (Hybrid) provides statistical expertise to support the research and development organization, specifically focusing on clinical trials, patient safety, and global medical affairs. The role involves independently developing protocols, statistical analysis plans, and product safety analysis plans while implementing sound statistical methodology in scientific investigations. Key responsibilities include identifying data collection instruments, performing statistical analyses, providing programming specifications for derived variables, and collaborating with Statistical Programming to deliver high-quality outputs. The position requires the ability to perform statistical computations and simulations, evaluate software appropriateness, and communicate complex concepts to non-statisticians. Candidates must possess an MS or PhD in Statistics or Biostatistics and have experience in drug development within a regulated environment, specifically addressing the technical challenges of oncology research and late phase trials.

Skills

Biostatistics Statistics Clinical Trials Statistical Analysis Plans Data Science Data Collection Simulations Drug Development

What you'll do

Design and develop protocols and statistical analysis plans for clinical trials and scientific research studies.
Implement sound statistical methodologies and provide programming specifications for derived variables and analysis datasets.
Identify scientifically appropriate data collection instruments and report data issues or violations of study assumptions.
Perform independent statistical analyses and collaborate with programming teams to ensure high-quality, timely outputs.
Evaluate software appropriateness and develop novel statistical methodologies for planned analyses.
Develop strategies for data presentation, inference, and the publication of scientific research.
Ensure the accuracy and internal consistency of tables, listings, figures, and scientific reports.
Explain complex statistical concepts to non-statisticians and provide responses to data-driven inquiries.

What we're looking for

MS with 6+ years of experience or a PhD with 2+ years of experience in Statistics, Biostatistics, or a related field.
Pharmaceutical experience or experience understanding drug development and life-cycle management in a regulated environment.
High degree of technical competence and effective oral and written communication skills.
Ability to perform statistical computations and simulations.
Ability to identify data or analytical issues and provide solutions through personal knowledge or collaboration.
Ability to build strong relationships with peers and cross-functional partners to drive innovation.
Oncology specific experience (preferred).
Late phase trial experience (preferred).

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