Senior Scientist, Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)
Join CSL’s R&D organization to accelerate innovation in therapy development. This role focuses on monitoring non‑clinical PK/TK studies and supporting modelling activities that drive regulatory submissions and drug development.
Responsibilities
Design, oversee, and interpret nonclinical PK/QSP studies (GLP and non‑GLP) to support regulatory submissions and drug development.
Conduct PK, PBPK, QSP modelling and collaborate with external partners.
Prepare and review regulatory nonclinical submission documents.
Collaborate with internal stakeholders including pharmacology, toxicology, clinical, regulatory, and CMC teams.
Qualifications
Bachelor’s, Master’s, or Ph.D. in Life Sciences or related field with at least 3 years of pharmaceutical development experience in pharma, biotech, or CRO.
Experience in PK/PD, modelling and simulation using industrystandard software (e.g., Phoenix WinNonLin, NONMEM, R).
Strong communication and cross‑functional collaboration skills.
Knowledge of CSL’s therapeutic areas is desirable.
Experience across multiple therapeutic areas and modalities is highly desirable.
Benefits
We encourage you to make your well‑being a priority. Learn more about how we care at CSL.
About CSL Behring
CSL Behring is a global biotherapeutics leader focused on delivering innovative therapies for patients worldwide. Our platforms include plasma fractionation, recombinant protein technology, and cell and gene therapy.
Inclusion & Belonging
At CSL, inclusion and belonging are at the core of our mission. By celebrating differences and fostering an environment of curiosity and empathy, we better serve our patients, donors, and the global community.
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