Senior Statistical Data Scientist

Overview

Hands-on Senior Statistical Data Scientist to deliver statistical programming outputs for clinical study reports and study/asset teams with limited supervision early and independence later.

What you'll do

• Deliver analysis-ready datasets, tables, listings, and figures for assigned areas.
• Ensure adherence to high-quality statistical programming standards.
• Provide quality and timely datasets and displays for clinical study reports and other deliverables.
• Maintain appropriate documentation and QC across the study lifecycle for programming outputs.
• Collaborate with statisticians and programming leads to ensure clear specifications for deliverables.
• Apply routine and occasionally complex problem-solving and seek direction when appropriate.

What you'll need

• 3+ years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
• Hands-on statistical programming experience.
• SAS hand-on experience.
• Clinical trials expertise with understanding of data operations for reporting clinical trial data.
• Good understanding of ICH and regulatory guidelines.
• Working knowledge of clinical data and relevant data standards.
• Bachelor’s or Master’s degree in Statistics, Biological Sciences, IT, or related field (Master’s preferred).

Details

• Work location assignment: Hybrid.