Target RWE aims to leverage real-world data to advance clinical research and inform better healthcare decisions. The business problem involves generating rigorous, reliable, and regulatory-grade real-world evidence to improve patient outcomes across life sciences, regulatory, and academic applications.
Requirements
- Advanced degree (PhD preferred) in biostatistics, epidemiology, health economics, bioinformatics, data science, or a related quantitative field
- 15+ years experience generating real-world evidence or clinical research insights, with demonstrated success leading scientific functions
- Demonstrated expertise in statistical methodology, reproducible analytic frameworks, and regulatory-grade evidence generation
- Proven ability to translate scientific objectives into scalable products, processes, and operational strategies
- Exceptional communication skills, with experience presenting to executive, scientific, and regulatory stakeholders
- Track record of mentoring and elevating high-performing teams
- Experience in developing and communicating scientific standards
Responsibilities
- Serve as the scientific owner of Target’s data assets and analytic frameworks
- Establish standards for data validation, methodology, reproducibility, and statistical rigor
- Develop scalable systems for data quality, curation, and 'fitness-for-use' demonstrability
- Champion regulatory-readiness and scientific credibility of Target’s data across audiences
- Oversee study design, statistical analysis plans, and analytic frameworks
- Guide development of reusable analytic modules and workflows across therapeutic areas
- Review and approve high-stakes analyses, publications, and client deliverables
Other
- Hybrid role located in Research Triangle Park, North Carolina
- Advanced degree (PhD preferred) in a relevant field
- Exceptional communication skills
- Experience presenting to executive, scientific, and regulatory stakeholders
- Ability to lead, grow, and develop a multidisciplinary team
