Senior Manager, Trial Surveillance & Analytics

AbbVie

Confirmed live today High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Irvine, CA
Salary
$124,500–$236,500 / yr
Posted
11 days ago
Freshness
Confirmed live today
Closes
Oct 15, 2126

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $190k
This role $180k
$111k $250k
below market most similar roles pay here above market

This role pays less than 51% of similar roles. Most pay $165,000–$214,900 — the blue band above. At the midpoint, this role pays about $180k versus about $190k 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 145 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 140 roles with salary data.

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At a glance

TL;DR · Senior Manager, Trial Surveillance & Analytics

The Senior Manager, Trial Surveillance & Analytics joins the Trial Surveillance & Analytics center of excellence within the Data and Statistical Sciences organization. As a hands-on, full-stack data scientist, you will own solutions from problem statement to production, building data pipelines and integrated databases on SDTM and ADaM to support safety and efficacy surveillance. You will design applications, dashboards, and self-service tools while applying generative and agentic AI to the analysis workflow. Key responsibilities include leading blinded analytics, automating reporting, and integrating clinical trial and real-world data. Required skills include proficiency in R, Python, SQL, and Git, along with experience in machine learning, statistics, and clinical data. You will solve the technical problem of detecting emerging safety signals early during ongoing clinical trials.

What you'll do

  • Frame surveillance problems with stakeholders to design solutions for early safety and efficacy signal detection.
  • Design and build data pipelines using SDTM, ADaM, and integrated databases for clinical trial analysis.
  • Lead blinded, standardized analytics across studies to identify emerging safety and efficacy signals.
  • Deliver and automate reporting, including tables, listings, figures, and safety reports.
  • Develop and deploy applications, dashboards, and self-service tools for study teams and patient safety colleagues.
  • Apply generative and agentic AI to the analysis workflow and build AI agents on clinical data foundations.
  • Integrate clinical trial and real-world data while assessing data quality and comparability.
  • Lead cross-functional projects and small pods while coaching and mentoring team members.

What we're looking for

  • MS with 8+ years of experience or PhD with 4+ years of experience in Statistics, Biostatistics, Bioinformatics, Machine Learning, AI, or a related field.
  • Experience in pharmaceutical, biotech, health technology, or related industries.
  • Strong hands-on programming in R, Python, SQL, and version control (e.g., Git) to write production-quality code for end-to-end analytical pipelines.
  • Demonstrated experience applying generative or agentic AI to analytical or programming work with measurable results.
  • Experience working with clinical trial data (e.g., CDISC SDTM/ADaM) and/or real-world data (e.g., EHR, claims, registries).
  • A track record of building analytical tools or solutions that were adopted and sustained by users.
  • Strong communication skills to explain technical concepts in plain language and influence cross-functional partners.
  • Experience designing and building agentic AI systems, clinical development, or building interactive visualizations with modern frameworks (preferred).

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