Sanofi-Aventis Deutschland GmbH
Translational T1/17 Immunology Lead(m/w/x)
Vollzeitnur vor OrtSenior
Frankfurt am Main
Neuer Job?Nejo!
Die KI-Suchmaschine für Jobs
SASanofi
Clinical Lead, Early Clinical and Experimental Therapeutics(m/w/x)
Frankfurt am Main
VollzeitVor OrtJunior
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 1 - 5 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- High-quality healthcare
Sonstige Vorteile
- Numerous prevention programs
- Coverage for long-term illness
Großzügige Elternzeit
- 14-week paid family leave
Kinderbetreuung
- Childcare benefits
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Sanofi erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- Fresenius Kabi Deutschland GmbH
(Junior) Manager Medical Study Development, IITs & Intelligence(m/w/x)
VollzeitBefristeter Vertragnur vor OrtJuniorBad Homburg vor der Höhe - Scholar Rock
Country Medical Director(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main, München - Roche Pharma AG
Global Medical Collaboration Leader - Cardiovascular(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Distinguished Scientist, Group Head Synthetic Medicinal Modalities(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main
SASanofi
Clinical Lead, Early Clinical and Experimental Therapeutics(m/w/x)
Frankfurt am Main
VollzeitVor OrtJunior
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 1 - 5 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- High-quality healthcare
Sonstige Vorteile
- Numerous prevention programs
- Coverage for long-term illness
Großzügige Elternzeit
- 14-week paid family leave
Kinderbetreuung
- Childcare benefits
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Sanofi erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
Sanofi
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein forschendes Biopharma-Unternehmen, das KI anwendet und sich dafür einsetzt, das Leben der Menschen zu verbessern.
Noch nicht perfekt?
- Sanofi-Aventis Deutschland GmbH
Translational T1/17 Immunology Lead(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main - Fresenius Kabi Deutschland GmbH
(Junior) Manager Medical Study Development, IITs & Intelligence(m/w/x)
VollzeitBefristeter Vertragnur vor OrtJuniorBad Homburg vor der Höhe - Scholar Rock
Country Medical Director(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main, München - Roche Pharma AG
Global Medical Collaboration Leader - Cardiovascular(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Distinguished Scientist, Group Head Synthetic Medicinal Modalities(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main