About this role
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Key Accountabilities: General Accountabilities • Responsible for the development and application of QSP models for the in-silico evaluation of novel targets and compounds, including preclinical and clinical study design and mechanistic interpretation of results. This individual integrates and shares data and knowledge in a highly stimulating, collaborative, and multi-disciplinary environment to develop a quantitative understanding of physiological systems and disease mechanisms within and across therapeutic areas.
Compliance with Parexel standards • Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required • Maintains a working knowledge of and complies with Parexel processes, ICH- GCPs and other applicable requirements
Skills: • Hands-on experience in developing QSP and/or differential equation-based models of biological or physiological systems.
Knowledge and Experience: • Minimum 1- 3 years relevant experience • Fluent in both oral and written English. • Fluent in host country language required
Education: • Ph.D. in Applied Mathematics, Engineering, Physics, Pharmaceutical Sciences, or related disciplines with strong background in mathematical, statistical, and numerical methods.