CSL Behring
Principal Scientist, Pharmacokinetics (PK)(m/w/x)
Full-timeOn-siteSenior
Glattbrugg
New Job?Nejo!
The AI Job Search Engine
CSCSL Behring
Senior Scientist, Pharmacokinetics (PK)(m/w/x)
Glattbrugg
Full-timeOn-siteSenior
Nejo AI Summary
Monitoring and interpreting non-clinical PK/TK/QSP studies for biotherapeutics development. 3+ years pharmaceutical development experience with pharmacokinetic modeling focus required. Advanced modeling software, cross-functional team collaboration.
Requirements
- Bachelor’s, Master’s, or Ph.D. in Life Sciences or related subject
- 3+ years pharmaceutical development experience (pharma, biotech, or CRO)
- Focus on modeling and simulation
- Training in PK/PD, modeling and simulation
- Excellent communication skills
- Cross-functional collaboration skills
- Experience with CSL’s disease therapeutic areas
- Highly desirable experience across multiple therapeutic areas and modalities
- Understanding of complex issues
Tasks
- Monitor non-clinical PK/TK studies (GLP/non-GLP)
- Support modeling activities
- Design nonclinical PK/QSP studies
- Oversee nonclinical PK/QSP studies
- Interpret nonclinical PK/QSP study results
- Support regulatory submissions and drug development
- Conduct PK, PBPK, QSP modeling
- Work with external collaborators
- Prepare regulatory nonclinical submission documents
- Review regulatory nonclinical submission documents
- Collaborate with internal stakeholders
- Manage projects and processes
- Work independently with limited supervision
- Coach lower-level professionals
- Review work of lower-level professionals
- Contribute to scientific experiment planning and execution
- Evaluate and report scientific experiments with integrity
- Collaborate with team members on research projects
- Provide expertise to team members
- Achieve research project objectives
Work Experience
- 3 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- Phoenix WinNonLin
- NONMEM
- R
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- CSL Behring
Associate Director, Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Director Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)(m/w/x)
Full-timeOn-siteSeniorOpfikon - CSL Behring
Director, Non-clinical Pharmacology CVR(m/w/x)
Full-timeOn-siteSeniorSchlieren - CSL Behring
Principal Scientist, Toxicology(m/w/x)
Full-timeOn-siteSeniorOpfikon
CSCSL Behring
Senior Scientist, Pharmacokinetics (PK)(m/w/x)
Glattbrugg
Full-timeOn-siteSenior
Nejo AI Summary
Monitoring and interpreting non-clinical PK/TK/QSP studies for biotherapeutics development. 3+ years pharmaceutical development experience with pharmacokinetic modeling focus required. Advanced modeling software, cross-functional team collaboration.
Requirements
- Bachelor’s, Master’s, or Ph.D. in Life Sciences or related subject
- 3+ years pharmaceutical development experience (pharma, biotech, or CRO)
- Focus on modeling and simulation
- Training in PK/PD, modeling and simulation
- Excellent communication skills
- Cross-functional collaboration skills
- Experience with CSL’s disease therapeutic areas
- Highly desirable experience across multiple therapeutic areas and modalities
- Understanding of complex issues
Tasks
- Monitor non-clinical PK/TK studies (GLP/non-GLP)
- Support modeling activities
- Design nonclinical PK/QSP studies
- Oversee nonclinical PK/QSP studies
- Interpret nonclinical PK/QSP study results
- Support regulatory submissions and drug development
- Conduct PK, PBPK, QSP modeling
- Work with external collaborators
- Prepare regulatory nonclinical submission documents
- Review regulatory nonclinical submission documents
- Collaborate with internal stakeholders
- Manage projects and processes
- Work independently with limited supervision
- Coach lower-level professionals
- Review work of lower-level professionals
- Contribute to scientific experiment planning and execution
- Evaluate and report scientific experiments with integrity
- Collaborate with team members on research projects
- Provide expertise to team members
- Achieve research project objectives
Work Experience
- 3 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- Phoenix WinNonLin
- NONMEM
- R
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
CSL Behring
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
Not a perfect match?
- CSL Behring
Principal Scientist, Pharmacokinetics (PK)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Associate Director, Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Director Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)(m/w/x)
Full-timeOn-siteSeniorOpfikon - CSL Behring
Director, Non-clinical Pharmacology CVR(m/w/x)
Full-timeOn-siteSeniorSchlieren - CSL Behring
Principal Scientist, Toxicology(m/w/x)
Full-timeOn-siteSeniorOpfikon