Project (Associate) - Development - Marburg, Deutschland - CSL Behring

Beschreibung

For our Research department, we are looking for a

As Principal PK & QSP Expert you will serve as the lead PKPD/ ADME/QSP project scientist for a variety of programs and drug modalities; You will provide scientific expertise and guidance in biologics research and development related activities and will be willing to evolve knowledge into novel areas of interest, such as gene therapy

You will lead study design discussions, study protocols development, including sample size calculations, data analysis plan, and report population PK and PK/PD analysis results to management and review committees
As expert in the field you will provide technical guidance and mentor junior team members to achieve the project objectives
A PhD in Pharmaceutical Sciences or related subject area with 6 years of pharmaceutical development experience in pharma, biotech, or CRO, with a focus on modeling and simulation OR

A master's degree in Pharmaceutical Sciences or related subject area with 8 years of pharmaceutical development experience in pharma, biotech, or CRO, with a focus on modeling and simulation.

Training in PK/PD, modelling and simulation, using industry standard software packages, such as Phoenix WinNonLin, NONMEM, R, etc
Demonstrated experience supporting projects using PK and PKPD capability
Innovative work-environment at our R&D campus
CSL-subsidized company bike leasing
For more information, please check out our global benefits below.

Please ensure to apply online with your CV and certifications as well as your salary expectation.

Our Benefits

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases.

As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion.