Senior Manager, Trial Surveillance & Analytics (Hybrid)

📋 Description

• Frame surveillance problems with stakeholders before building: understand the decision to be
• Design and build data pipelines and analysis-ready, integrated data on SDTM, ADaM and integrated
• Lead blinded, standardized analytics across studies and compounds to detect emerging safety and
• Deliver reporting — tables, listings and figures, safety reports and listings — and automate it
• Develop applications, dashboards and self-service tools that study teams and patient safety
• Apply generative and agentic AI across the analysis workflow, build AI agents on the clinical data

🎯 Requirements

• MS (with 8+ years of experience) or PhD (with 4+ years of experience) in Statistics, Biostatistics
• Experience may be in pharmaceutical, biotech, health technology or related industries.
• Strong hands-on programming in R and Python, plus SQL and version control (e.g. Git), with a track
• Demonstrated experience applying generative or agentic AI to analytical or programming work, with
• Experience working with clinical trial data (e.g. CDISC SDTM/ADaM) and/or real-world data (e.g.
• A track record of building analytical tools or solutions that were adopted and sustained by their

🎁 Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Long-term incentive programs
• Hybrid work schedule (Tuesday-Thursday onsite; Mondays & Fridays remote)