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.

Quantitative Systems Pharmacologist (FSP)

Parexel

Job Description

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