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Associate Director, Non-Clinical Pharmacology - CVR(m/w/x)
Designing and implementing PK/PD and efficacy study protocols for biotherapeutics. 5+ years nonclinical pharmacology experience required. Well-being support, collaboration with internal and external partners.
Requirements
- Ph.D. in Pharmacology, Physiology, Biomedical Sciences, or related field
- 5+ years nonclinical pharmacology experience in pharma/biotech
- Proven understanding of drug discovery and development
- Expertise in in vivo pharmacology
- Expertise in disease models
- Expertise in translational science for Cardiovascular/Renal Disease Biology
- Experience across multiple therapeutic areas and modalities
- Ability to work in project teams
- Ability to manage multiple projects and timelines
Tasks
- Design and implement PK/PD and efficacy study protocols
- Work with PK, Toxicology, and Translational Science teams
- Collaborate with internal and external partners for study execution
- Manage and guide third-party vendors and experiments
- Participate in project teams and provide expert input
- Prepare and present study reports and findings
- Contribute to regulatory documents for IND submission
- Foster a culture of scientific excellence and innovation
Work Experience
- 5 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Benefits
Mental Health Support
- Well-being support
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Associate Director, Non-Clinical Pharmacology - CVR(m/w/x)
Designing and implementing PK/PD and efficacy study protocols for biotherapeutics. 5+ years nonclinical pharmacology experience required. Well-being support, collaboration with internal and external partners.
Requirements
- Ph.D. in Pharmacology, Physiology, Biomedical Sciences, or related field
- 5+ years nonclinical pharmacology experience in pharma/biotech
- Proven understanding of drug discovery and development
- Expertise in in vivo pharmacology
- Expertise in disease models
- Expertise in translational science for Cardiovascular/Renal Disease Biology
- Experience across multiple therapeutic areas and modalities
- Ability to work in project teams
- Ability to manage multiple projects and timelines
Tasks
- Design and implement PK/PD and efficacy study protocols
- Work with PK, Toxicology, and Translational Science teams
- Collaborate with internal and external partners for study execution
- Manage and guide third-party vendors and experiments
- Participate in project teams and provide expert input
- Prepare and present study reports and findings
- Contribute to regulatory documents for IND submission
- Foster a culture of scientific excellence and innovation
Work Experience
- 5 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Benefits
Mental Health Support
- Well-being support
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
CSL Behring AG (CH)
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein weltweit führendes Biotech-Unternehmen, das lebensrettende Therapien für Menschen mit schweren und seltenen Krankheiten entwickelt und vertreibt.
Not a perfect match?
- CSL Behring
Director, Non-clinical Pharmacology CVR(m/w/x)
Full-timeOn-siteSeniorSchlieren - CSL Behring
Associate Director, Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring AG (CH)
Associate Director Translational Research CVR(m/w/x)
Full-timeOn-siteManagementSchlieren - CSL Behring
Director Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)(m/w/x)
Full-timeOn-siteSeniorOpfikon - CSL Plasma
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Full-timeOn-siteManagementSchlieren