- Serves as the lead PKPD/ ADME/QSP project scientist for a variety of programs and drug modalities; biologics, small molecules and novel platforms such as cell- and gene-therapy, gene-editing, and non-viral gene delivery
- Serves as technical expert for the PK/QSP organization in the application of advanced PK/PD, mechanistic, and disease modeling principles and methodologies,
- Performs advanced PK/PD modeling utilizing mechanistic and semi-mechanistic approaches to define the dose-concentration-efficacy/toxicity relationships, formulate various study design scenarios, and outcome prediction, to inform decision making,
- Leads 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
- 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.
- You will work in an international environment
Ihr Kontakt
Referenznummer
782272/1
Kontakt aufnehmen
Telefon:+ 49 621 1788-4297
E-Mail: positionen@hays.de
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