Job description
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.