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Clinical Lead, Early Clinical and Experimental Therapeutics(m/w/x)
Designing First-In-Human studies and ECET plans for an AI-driven research biopharma. Experience in late phase clinical trials required. 14-week paid family leave, childcare benefits.
Requirements
- Experience in basic science, translational medicine, and/or clinical research
- Knowledge and mindset in translational research
- Experience in the conduct of late phase clinical trials
- Very good communication skills (verbal and written)
- Demonstrated capability to challenge decisions and status quo
- Ability to work within a matrix organization
- International/intercultural working skills
- Open-minded to apply new digital and/or AI-driven solutions
- Advanced degree: M.D. or M.D./Ph.D with at least 1-5 years of research experience
- Broad immunology knowledge base
- Able to acquire and apply new technical skills
- Postgraduate residency training; laboratory research in industry or academia is a plus
- Fluent in English
Tasks
- Design early development and ECET plans
- Create safe and informative First-In-Human studies
- Supervise study execution and medical monitoring
- Review and interpret clinical results
- Author ECET-related clinical documentation
- Interact with cross-functional managers and partners
- Participate in dose selection for First-In-Human studies
- Ensure follow-up on studies and project timelines
- Present data at internal and external meetings
- Emphasize strengths of the TMU and Clinical Patient Sciences
- Engage in scientific challenges of early clinical development
- Maintain Clinical Trial standards and communication processes
- Produce high-quality documents with strong writing skills
- Manage timelines through cross-functional planning
- Make decisions on protocol design and safety
- Design and conduct early clinical development studies
- Review and approve study documentation
- Coordinate clinical team for study setup
- Ensure documentation for Ethics Committees and Health Authorities
- Ensure scientific soundness of study conduct
- Prepare and review interim investigator reports
- Lead Dose Escalation Meetings and document decisions
- Review Adverse Event reports
- Participate in data review and validation meetings
- Prepare Key Results Memo and Clinical Study Report
Work Experience
- 1 - 5 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
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 Lead, Early Clinical and Experimental Therapeutics(m/w/x)
Designing First-In-Human studies and ECET plans for an AI-driven research biopharma. Experience in late phase clinical trials required. 14-week paid family leave, childcare benefits.
Requirements
- Experience in basic science, translational medicine, and/or clinical research
- Knowledge and mindset in translational research
- Experience in the conduct of late phase clinical trials
- Very good communication skills (verbal and written)
- Demonstrated capability to challenge decisions and status quo
- Ability to work within a matrix organization
- International/intercultural working skills
- Open-minded to apply new digital and/or AI-driven solutions
- Advanced degree: M.D. or M.D./Ph.D with at least 1-5 years of research experience
- Broad immunology knowledge base
- Able to acquire and apply new technical skills
- Postgraduate residency training; laboratory research in industry or academia is a plus
- Fluent in English
Tasks
- Design early development and ECET plans
- Create safe and informative First-In-Human studies
- Supervise study execution and medical monitoring
- Review and interpret clinical results
- Author ECET-related clinical documentation
- Interact with cross-functional managers and partners
- Participate in dose selection for First-In-Human studies
- Ensure follow-up on studies and project timelines
- Present data at internal and external meetings
- Emphasize strengths of the TMU and Clinical Patient Sciences
- Engage in scientific challenges of early clinical development
- Maintain Clinical Trial standards and communication processes
- Produce high-quality documents with strong writing skills
- Manage timelines through cross-functional planning
- Make decisions on protocol design and safety
- Design and conduct early clinical development studies
- Review and approve study documentation
- Coordinate clinical team for study setup
- Ensure documentation for Ethics Committees and Health Authorities
- Ensure scientific soundness of study conduct
- Prepare and review interim investigator reports
- Lead Dose Escalation Meetings and document decisions
- Review Adverse Event reports
- Participate in data review and validation meetings
- Prepare Key Results Memo and Clinical Study Report
Work Experience
- 1 - 5 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
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
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein forschendes Biopharma-Unternehmen, das KI anwendet und sich dafür einsetzt, das Leben der Menschen zu verbessern.
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