CSL Behring
Associate Director, Hematology(m/w/x)
Full-timeOn-siteSenior
Schlieren
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CSCSL Behring AG (CH)
Associate Director Translational Research CVR(m/w/x)
Schlieren
Full-timeOn-siteManagement
Nejo AI Summary
At a global biotech developing therapies for severe and rare diseases, designing and overseeing CVR biomarker studies. PhD/MD-PhD with 8-10 years industry/academic experience and strong biomarker discovery track record required. Cross-functional team collaboration.
Requirements
- PhD, MD-PhD, or equivalent in relevant discipline
- Expertise in diseases relevant to CSL’s TA Strategies
- 8–10 years of relevant industry or academic experience
- Strong track record in translational research
- Expertise in biomarker discovery and study design
- Experience integrating clinical and scientific data
- Knowledge of epidemiological and statistical methods
- Leadership and people management skills
- Excellent communication and strategic thinking skills
- Experience in regulatory documentation and scientific writing
- Ability to work in international teams
Tasks
- Design and oversee cardiovascular and renal biomarker studies
- Develop protocols and manage data analysis for non-interventional research
- Create biomarker strategies for toxicology and early clinical trials
- Integrate real-world evidence and systematic literature reviews
- Lead mechanism of action and target validation studies
- Coordinate with internal pharmacology units and external academic partners
- Provide scientific guidance to preclinical and clinical R&D projects
- Represent translational research in global cross-functional core teams
- Contribute to regulatory submissions and scientific publications
- Supervise and mentor research scientists within the pharmacology units
- Support contract negotiations and patent filings with legal teams
- Maintain quality management standards and compliance
- Provide strategic input for early-phase project due diligence
Work Experience
- 8 - 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Tools & Technologies
- Epidemiological methods
- Statistical methods
- Regulatory documentation
Benefits
Informal Culture
- Inclusion and belonging culture
Other Benefits
- Reasonable disability accommodations
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring AG (CH) 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.
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CSCSL Behring AG (CH)
Associate Director Translational Research CVR(m/w/x)
Schlieren
Full-timeOn-siteManagement
Nejo AI Summary
At a global biotech developing therapies for severe and rare diseases, designing and overseeing CVR biomarker studies. PhD/MD-PhD with 8-10 years industry/academic experience and strong biomarker discovery track record required. Cross-functional team collaboration.
Requirements
- PhD, MD-PhD, or equivalent in relevant discipline
- Expertise in diseases relevant to CSL’s TA Strategies
- 8–10 years of relevant industry or academic experience
- Strong track record in translational research
- Expertise in biomarker discovery and study design
- Experience integrating clinical and scientific data
- Knowledge of epidemiological and statistical methods
- Leadership and people management skills
- Excellent communication and strategic thinking skills
- Experience in regulatory documentation and scientific writing
- Ability to work in international teams
Tasks
- Design and oversee cardiovascular and renal biomarker studies
- Develop protocols and manage data analysis for non-interventional research
- Create biomarker strategies for toxicology and early clinical trials
- Integrate real-world evidence and systematic literature reviews
- Lead mechanism of action and target validation studies
- Coordinate with internal pharmacology units and external academic partners
- Provide scientific guidance to preclinical and clinical R&D projects
- Represent translational research in global cross-functional core teams
- Contribute to regulatory submissions and scientific publications
- Supervise and mentor research scientists within the pharmacology units
- Support contract negotiations and patent filings with legal teams
- Maintain quality management standards and compliance
- Provide strategic input for early-phase project due diligence
Work Experience
- 8 - 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Tools & Technologies
- Epidemiological methods
- Statistical methods
- Regulatory documentation
Benefits
Informal Culture
- Inclusion and belonging culture
Other Benefits
- Reasonable disability accommodations
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring AG (CH) 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.
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
Associate Director, Hematology(m/w/x)
Full-timeOn-siteSeniorSchlieren - CSL Behring
Senior Director, Head of Translational Research Hematology & CVR(m/w/x)
Full-timeOn-siteManagementSchlieren - CSL Behring
Director, Non-clinical Pharmacology CVR(m/w/x)
Full-timeOn-siteSeniorSchlieren - CSL Behring
Senior Director Global Clinical Program Lead Cardiovascular & Renal(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - CSL Behring
Associate Director, Pharmacokinetics (PK) & Quantitate Systems Pharmacology (QSP)(m/w/x)
Full-timeOn-siteSeniorGlattbrugg