Senior Manager, Trial Surveillance & Analytics; Hybrid

• Full-time
• Salary Min: 124500
• Salary Max: 236500
• Workday Global Grade: 19
• Compensation: USD 124,500 - USD 236,500 - yearly

About Abb Vie

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  .

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Trial Surveillance & Analytics (TSA) is a newly formed center of excellence in Data & AI Acceleration, part of Abb Vie's Data and Statistical Sciences organization. Our mission is to transform how Abb Vie conducts ongoing clinical trial surveillance — integrating trial data, analytics and AI so that study teams and patient safety colleagues see emerging safety and efficacy signals early, and can act on them with confidence.

This is work upstream, inside ongoing clinical trials, where insight can still change decisions for the study and for patients.

The Senior Manager, Trial Surveillance & Analytics is a hands‑on, full‑stack data scientist who takes a surveillance question from intake to a working solution. You will work in a small team that owns a capability end to end — from the data, through the analysis, to the tool that study teams use — and you will own your solutions from problem statement to a working product that people use.

The team is AI‑native from day one: agentic coding and AI agents are part of how we work, with room to experiment and to scale what works. You will combine depth in one area (such as statistical programming and reporting, data integration, data visualization, data science and machine learning, or data and software engineering) with enough breadth across clinical data, analytics and AI to deliver on your own, with the support of the team.

As an early member of a new center of excellence, you will help define how it works, the standards it sets and the capabilities it builds, partnering across Global Patient Safety, therapeutic area clinical development teams, Statistics, Statistical Programming and data engineering across the portfolio.

Key Responsibilities:

• Frame surveillance problems with stakeholders before building: understand the decision to be supported, design for adoption, and iterate with users.
• Design and build data pipelines and analysis-ready, integrated data on SDTM, ADaM and integrated databases to support safety and efficacy surveillance.
• Lead blinded, standardized analytics across studies and compounds to detect emerging safety and efficacy signals early.
• Deliver reporting — tables, listings and figures, safety reports and listings — and automate it wherever possible.
• Develop applications, dashboards and self‑service tools that study teams and patient safety colleagues use themselves; drive their adoption and measure their use.
• Apply generative and agentic AI across the analysis workflow, build AI agents on the clinical data foundation, and measure the gain in time and quality.
• Integrate clinical trial and real‑world data where the science requires it, assessing comparability and data quality first.
• Lead projects and small cross‑functional pods; coach and mentor team members. May include indirect supervision of employees and contract staff.
• Represent the team in cross‑functional forums and communicate technical concepts and results clearly to non‑technical audiences.
• Ensure adherence to applicable regulations, Good Clinical Practice (GCP), ICH guidelines, Abb Vie Standard Operating Procedures…