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Clinical Study Unit (CSU) Cluster Head GSA(m/w/x)
Overseeing clinical study operations for cardiovascular disease prevention medicines at pharmaceutical company focused on cardiovascular health. Proven track record in cross-functional leadership and people management required. 14-week paid family leave.
Requirements
- Advanced knowledge of drug development and clinical trial design
- Proven track record in cross-functional leadership and people management
- Strong understanding of ICH-GCP and regulatory requirements
- Advanced business acumen and strategic planning capabilities
- Experience in budget management and risk assessment
- Change management expertise and digital innovation mindset
- Strong analytical and problem-solving abilities
- In-depth knowledge of local clinical trial ecosystem
- Demonstrated ability to build and maintain relationships with regulators and healthcare professionals
- Experience in influencing local stakeholders and driving country strategies
- Understanding of local healthcare landscape and regulatory environment
- University degree, postgraduate Master's or PhD in nature science, pharmacy, medicine or related
- English and German business fluent
Tasks
- Manage and optimize clinical study operations across Germany, Switzerland, and Austria
- Oversee the delivery of clinical trials in the GSA cluster
- Ensure clinical studies meet deadlines, quality standards, and cost efficiency
- Align cluster countries with strategic company priorities
- Develop cluster strategy in line with global clinical development plans
- Lead internal and external representation for CSO/R&D in the cluster
- Define strategy for implementing the clinical study pipeline
- Establish business development strategies with key investigators and KOLs
- Provide clinical development expertise for post-marketing studies
- Integrate medical and scientific intelligence into global development strategy
- Foster digital innovation and drive change management with medical communities
- Define future strategies for clinical trials and business evolution
- Contribute to global CSU and CSO workstreams
- Optimize quality, cost efficiency, and speed of clinical studies
- Support the development of the Regional CSU business strategy
- Participate in the Cluster/MCO Medical Leadership Team and MRPQ as needed
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Flexible Working
- Hybrid working time models
Healthcare & Fitness
- High-quality healthcare
Other Benefits
- Numerous prevention programs
- Coverage for long-term illness
Generous Parental Leave
- 14-week paid family leave
Childcare
- Childcare benefits
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Clinical Study Unit (CSU) Cluster Head GSA(m/w/x)
Overseeing clinical study operations for cardiovascular disease prevention medicines at pharmaceutical company focused on cardiovascular health. Proven track record in cross-functional leadership and people management required. 14-week paid family leave.
Requirements
- Advanced knowledge of drug development and clinical trial design
- Proven track record in cross-functional leadership and people management
- Strong understanding of ICH-GCP and regulatory requirements
- Advanced business acumen and strategic planning capabilities
- Experience in budget management and risk assessment
- Change management expertise and digital innovation mindset
- Strong analytical and problem-solving abilities
- In-depth knowledge of local clinical trial ecosystem
- Demonstrated ability to build and maintain relationships with regulators and healthcare professionals
- Experience in influencing local stakeholders and driving country strategies
- Understanding of local healthcare landscape and regulatory environment
- University degree, postgraduate Master's or PhD in nature science, pharmacy, medicine or related
- English and German business fluent
Tasks
- Manage and optimize clinical study operations across Germany, Switzerland, and Austria
- Oversee the delivery of clinical trials in the GSA cluster
- Ensure clinical studies meet deadlines, quality standards, and cost efficiency
- Align cluster countries with strategic company priorities
- Develop cluster strategy in line with global clinical development plans
- Lead internal and external representation for CSO/R&D in the cluster
- Define strategy for implementing the clinical study pipeline
- Establish business development strategies with key investigators and KOLs
- Provide clinical development expertise for post-marketing studies
- Integrate medical and scientific intelligence into global development strategy
- Foster digital innovation and drive change management with medical communities
- Define future strategies for clinical trials and business evolution
- Contribute to global CSU and CSO workstreams
- Optimize quality, cost efficiency, and speed of clinical studies
- Support the development of the Regional CSU business strategy
- Participate in the Cluster/MCO Medical Leadership Team and MRPQ as needed
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Flexible Working
- Hybrid working time models
Healthcare & Fitness
- High-quality healthcare
Other Benefits
- Numerous prevention programs
- Coverage for long-term illness
Generous Parental Leave
- 14-week paid family leave
Childcare
- Childcare benefits
About the Company
Sanofi-Aventis Deutschland GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen bietet Arzneimittel zur Prävention von Herz-Kreislauf-Erkrankungen an und setzt sich für die Verbesserung der Lebensqualität ein.
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