Octapharma
Group Senior Manager R&D Applications(m/w/x)
Full-timeOn-siteSenior
Lachen
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Strategic leadership for global clinical development of human proteins from plasma and cell lines, at a global biopharmaceutical developer. Extensive experience in global clinical development strategy and program leadership required. High level of influence in long-term portfolio strategy.
Requirements
- Advanced degree in Medicine, Pharmacy, Life Sciences, or related field
- Extensive experience in clinical development strategy
- Track record in leading global clinical programs
- Expertise in regulatory frameworks and submissions
- High-level scientific leadership and evidence generation
- Strategic thinking and scientific judgment
- Experience managing budgets and resource allocation
- Ability to represent organization in senior-level interactions
- Fluency in English
Tasks
- Provide strategic leadership for global clinical development
- Contribute to long-term portfolio strategy
- Guide evidence-generation planning
- Lead cross-functional scientific teams
- Collaborate with international stakeholders
- Oversee external partners and governance bodies
- Provide guidance for early and late-stage development
- Review study concepts and regulatory documentation
- Represent the organization in scientific forums
- Refine clinical study plans for scientific integrity
- Resolve issues during study execution
- Plan timelines, resourcing, and budgets
- Align clinical, regulatory, and medical affairs functions
- Refine team roles and scientific capabilities
- Select and manage CROs and external partners
- Author key clinical and regulatory documents
- Create high-quality scientific presentations and submissions
Work Experience
- approx. 4 - 6 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Tools & Technologies
- ICH
- GCP
- EMA
- FDA
- IND
- IMPD
- CTD modules
Benefits
Competitive Pay
- Market-related salary and benefits
Job Security
- Long-term employee perspective
Purpose-Driven Work
- High level of influence
Informal Culture
- Skilled and fun colleagues
- Informal organization
Learning & Development
- Internal and external trainings
- Leadership trainee programs
- Digital learning solutions
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Octapharma 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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Strategic leadership for global clinical development of human proteins from plasma and cell lines, at a global biopharmaceutical developer. Extensive experience in global clinical development strategy and program leadership required. High level of influence in long-term portfolio strategy.
Requirements
- Advanced degree in Medicine, Pharmacy, Life Sciences, or related field
- Extensive experience in clinical development strategy
- Track record in leading global clinical programs
- Expertise in regulatory frameworks and submissions
- High-level scientific leadership and evidence generation
- Strategic thinking and scientific judgment
- Experience managing budgets and resource allocation
- Ability to represent organization in senior-level interactions
- Fluency in English
Tasks
- Provide strategic leadership for global clinical development
- Contribute to long-term portfolio strategy
- Guide evidence-generation planning
- Lead cross-functional scientific teams
- Collaborate with international stakeholders
- Oversee external partners and governance bodies
- Provide guidance for early and late-stage development
- Review study concepts and regulatory documentation
- Represent the organization in scientific forums
- Refine clinical study plans for scientific integrity
- Resolve issues during study execution
- Plan timelines, resourcing, and budgets
- Align clinical, regulatory, and medical affairs functions
- Refine team roles and scientific capabilities
- Select and manage CROs and external partners
- Author key clinical and regulatory documents
- Create high-quality scientific presentations and submissions
Work Experience
- approx. 4 - 6 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Tools & Technologies
- ICH
- GCP
- EMA
- FDA
- IND
- IMPD
- CTD modules
Benefits
Competitive Pay
- Market-related salary and benefits
Job Security
- Long-term employee perspective
Purpose-Driven Work
- High level of influence
Informal Culture
- Skilled and fun colleagues
- Informal organization
Learning & Development
- Internal and external trainings
- Leadership trainee programs
- Digital learning solutions
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Octapharma 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
Octapharma
Industry
Pharmaceuticals
Description
Das Unternehmen ist eines der weltweit größten, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt.
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