Manager, Statistics, Oncology

AbbVie

Confirmed live yesterday High trust
Hybrid

Quick summary

Work type
Hybrid
Location
South San Francisco, CA
Salary
$109,500–$208,500 / yr
Posted
2 days ago
Freshness
Confirmed live yesterday
Closes
Oct 8, 2126

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

The Manager, Statistics - Oncology (Hybrid) provides statistical expertise to the research and development organization, supporting clinical trials, patient safety, and global medical affairs. This role involves independently developing protocols, statistical analysis plans, and product safety analysis plans while implementing sound statistical methodology in scientific investigations. The successful candidate will identify data collection instruments, perform statistical analyses, and provide programming specifications for derived variables. Key responsibilities include collaborating with Statistical Programming to deliver high-quality outputs, developing data presentation strategies, and communicating complex statistical concepts to non-statisticians. Required skills include performing statistical computations and simulations, and possessing a deep understanding of drug development and life-cycle management in a regulated environment. The work focuses on advancing medicines through rigorous scientific research and evidence generation.

What you'll do

  • Develop protocols and statistical analysis plans for clinical trials and scientific research studies.
  • Implement sound statistical methodologies for scientific investigations and data analysis.
  • Identify appropriate data collection instruments and report issues or violations of study assumptions.
  • Provide programming specifications for derived variables and analysis datasets to the Data Science team.
  • Perform independent statistical analyses and collaborate with programming teams to ensure timely delivery of high-quality outputs.
  • 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 guidance on suggested analyses.

What we're looking for

  • MS with 6+ years of experience or PhD with 2+ years of experience in Statistics, Biostatistics, or a highly related field.
  • Pharmaceutical experience or experience and understanding of drug development and life-cycle management in a regulated environment.
  • High degree of technical competence and effective communication skills, both oral and written.
  • Ability to perform statistical computations and simulations.
  • Ability to identify data or analytical issues and provide solutions using own skills or by seeking help from others.
  • Ability to build strong relationships with peers and cross-functional partners to achieve higher performance.
  • Oncology specific experience (preferred).
  • Late phase trial experience (preferred).

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