Principal RWE Scientist

Job Summary

Providing strategic and operational support for real-world evidence generation, the contract remote Principal RWE Scientist will focus on the design and execution of external control arms and complex observational studies to inform regulatory and clinical decision-making.

Key responsibilities

• Design, execute, and communicate real-world evidence studies across the product lifecycle
• Ensure RWE studies meet regulatory, HTA, payer, and clinical decision-making requirements
• Mentor team members on RWE methodology and engage with external collaborators and data vendors

Required qualifications

• Doctoral degree in Epidemiology or related discipline with 8+ years of relevant experience, or a Master's degree with 10+ years of relevant experience
• Deep understanding of observational study design, causal inference, and real-world data sources
• Strong technical reading and writing skills
• Prior corporate experience in the hematology/oncology therapeutic area is highly preferred
• Minimum of four years of professional experience in the biopharmaceutical industry is preferred