Sanofi

biopharma

GroupHeadofQuantitativePharmacology-Projects,Germany

€114–171k Germany FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Group Head of Quantitative Pharmacology-Projects, Germany at Sanofi. Skills: Quantitative Pharmacology, Translational Medicine, R&D project leadership, team management. Lead strategy and execution of Translational Medicine and Quantitative Pharmacology programs supporting in-licensing, global R&D projects, and product registration. Manage and mentor a Quantitative Pharmacology team in Germany focused on dose and regimen selection, study design, drug-drug interaction assessment, benefit-risk eval”

What You'll Achieve.

advance our innovative pipeline; shape translational medicine strategy; transform patient lives and shapes regulatory strategies for innovative medicines

Industry & Context.

biopharma

What They're Looking For.

Must Have

PhD in pharmaceutical sciences or equivalent discipline, Minimum 12 years of industry experience in DMPK, PK/PD, pharmacometrics, or clinical pharmacology, Proven experience managing direct and indirect reports in academic or industry settings, Outstanding track record of peer-reviewed scientific publications and presentations at internationally recognized conferences, Experience with regulatory interactions (especially FDA and EMA) supporting multiple submissions, Fluency in English required

Nice to Have

PhD in pharmacokinetics, pharmacometrics, clinical pharmacology, or related field

What You'll Do.

Lead strategy and execution of Translational Medicine and Quantitative Pharmacology programs supporting in-licensing

and product registration

Manage and mentor a Quantitative Pharmacology team in Germany focused on dose and regimen selection

drug-drug interaction assessment

benefit-risk evaluation

and formulation development

Oversee development and review of protocols

and study reports for pharmacokinetic

and physiologically-based PK analyses

Provide strategic input and participate in health authority interactions at key regulatory milestones

Ensure compliance with legal and company safety regulations

including regular communication of workplace safety topics and conducting safety training based on risk assessments

How You'll Work.

Team & Collaboration

cross-functional collaboration abilities

Communication Scope

Excellent written and verbal communication skills

Process & Methodology

Lead strategic pharmacology programs supporting global R&D projects from in-licensing through registration

Full Job Description

**_About the job_** As Group Head of Quantitative Pharmacology-Projects, Germany within our Translational Medicine & Early Development team, you'll lead strategic pharmacology programs supporting global R&D projects from in-licensing through registration. Ready to get started? Based in Germany, you'll join our R&D organization where we leverage deep scientific expertise and cutting-edge pharmacology to advance our innovative pipeline. This leadership role offers the opportunity to shape translational medicine strategy while developing the next generation of quantitative pharmacology talent. **About Sanofi** We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives. **Main responsibilities:** * Lead strategy and execution of Translational Medicine and Quantitative Pharmacology programs supporting in-licensing, global R&D projects, and product registration * Manage and mentor a Quantitative Pharmacology team in Germany focused on dose and regimen selection, study design, drug-drug interaction assessment, benefit-risk evaluation, and formulation development * Oversee development and review of protocols, analysis plans, and study reports for pharmacokinetic, PK/PD, population PK, and physiologically-based PK analyses * Provide strategic input and participate in health authority interactions at key regulatory milestones * Ensure compliance with legal and company safety regulations, including regular communication of workplace safety topics and conducting safety training based on risk assessments **About you** Experience: * PhD in pharmaceutical sciences or equivalent discipline * Minimum 12 years of industry experience in DMPK, PK/PD, pharmacometrics, or clinical phar

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