Tech Stack

Description

You will build and lead a real-world data and analytics team, develop RWD strategies, and oversee studies supporting regulatory submissions and product value evidence for a clinical-stage oncology company.

Requirements

• PhD/DSc/DrPH in epidemiology or biostatistics or relevant advanced science degree
• At least 12 years of experience with RWD analytics and evidence generation in pharma/biotech
• Demonstrated experience leading complex RWD/RWE projects from concept through delivery
• Strong expertise with RWD sources and analytic tools (R/SAS/Python)
• Knowledge of drug and clinical development process for genomic/targeted medicines

Responsibilities

• Develop and lead RWD and analytics plans to support portfolio, Medical Affairs, HEOR/RWE, and epidemiology goals
• Oversee RWE study design, protocol development, statistical analysis, and reporting for regulatory submissions
• Provide subject matter expertise on RWD data sources and feasibility of answering scientific questions
• Communicate insights to senior stakeholders, regulatory agencies, payers, and scientific audiences
• Build, mentor, and lead a high-performing analytics team with expertise in epidemiology, biostatistics, and data science