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Pharmacometrician (all genders)

Bodman-Ludwigshafen
AbbVie
Inserat online seit: Veröffentlicht vor 3 Std.
Beschreibung

Stellenbeschreibung People. Passion. Possibilities. Three words that make a world of difference. More than a job. It's a chance to make a real difference. Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place! Together, we break through – as Pharmacometrician (all genders) (fixed-term 24 months) Pharmacometrics is concerned with the mathematical and statistical analyses and modeling of biological, pharmacological, and physiological data and processes. It quantifies the various aspects of the (desired and undesired) effects of drugs in the context of disease. The models are based on clinical data, and provide a basis for informing efficient drug development, regulatory decisions, and optimal treatment of patients. In this role you execute statistical and mathematical models that achieve projects, Clinical Pharmacology and Pharmacometrics goals. Your’re also responsible for implementing PK/PD modeling and simulation ideas as well as critically evaluate relevant Pharmacometric, PK/PD, Clinical Pharmacology and regulatory advances and integrate this knowledge into Clinical Pharmacology strategy for research or development programs. Make your mark : Contribute to clinical development by supporting Phase 1-4 studies with data analysis, modeling, and simulation evaluations to guide study design, and clinical pharmacology strategy. Actively participating in and presenting at ClinPharm project team meetings and to ClinPharm leadership. Contribute to regulatory documents including analysis plans, study reports, population PK reports, exposure-response analyses reports, common technical documents, white papers, and other similar documents. Seeking to continually evaluate and implement novel PMx methods and approaches. Delivering results for business needs and plays a role in positioning AbbVie for long-term success.

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