Merz Aesthetics GmbH
Clinical Quality Manager(m/w/x)
Vollzeitmit HomeofficeSenior
Frankfurt am Main
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
MEMerz Aesthetics GmbH
Medical / Scientific Expert, Clinical Development(m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Clinical trial design, set-up, execution, and reporting for aesthetic medicine products. 3+ years in clinical development/research required. Company day care centers, flexible working time.
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Anforderungen
- Master’s degree in Life Sciences; PhD or MD advantageous
- 3+ years experience in clinical development/research
- Strong scientific and regulatory writing skills
- Solid understanding of global clinical development, trial methodologies, and regulatory frameworks
- Experience collaborating with multidisciplinary, international teams
- Experience managing multiple priorities simultaneously
- Strong problem-solving skills
- Proactive challenge addressing in dynamic environments
- High levels of ownership
- Resilience and adaptability in fast-paced settings
- Professional stakeholder engagement
- Emotional intelligence and collaborative mindset
- Comfortable with Microsoft Office tools
- Comfortable with clinical documentation systems
- Clear and effective communication of complex scientific data
- Fluent English communication (written and presentations)
Aufgaben
- Contribute scientific and strategic expertise to clinical trial design
- Contribute scientific and strategic expertise to clinical trial set-up
- Contribute scientific and strategic expertise to clinical trial execution
- Contribute scientific and strategic expertise to clinical trial reporting
- Collaborate with cross-functional and international teams
- Shape clinical development strategies for devices, drugs, biologics, and combination products
- Integrate and interpret data from internal studies
- Integrate and interpret data from external research
- Integrate and interpret data from scientific literature
- Author high-quality clinical documents
- Review high-quality clinical documents
- Approve high-quality clinical documents
- Ensure clinical documentation complies with global and regional regulations
- Ensure clinical documentation complies with GCP
- Ensure clinical documentation complies with ICH guidelines
- Ensure clinical documentation complies with ISO standards
- Ensure clinical documentation complies with internal SOPs
- Provide scientific input into regulatory interactions
- Provide scientific input into regulatory submissions
- Support the selection of clinical outcome assessments
- Support the development of clinical outcome assessments
- Support the validation of clinical outcome assessments
- Identify risks in clinical development
- Troubleshoot scientific issues
- Troubleshoot operational issues
- Propose solutions to keep projects on track
- Prepare clinical trial results for internal stakeholders
- Present clinical trial results to internal stakeholders
- Prepare clinical trial results for scientific forums
- Present clinical trial results for scientific forums
- Prepare clinical trial results for external partners
- Present clinical trial results for external partners
- Support the publication of clinical data
- Contribute to abstracts
- Contribute to manuscripts
- Contribute to conference presentations
- Oversee external medical writing vendors
- Manage external medical writing vendors
- Contribute to process improvements in clinical development
- Contribute to internal trainings in clinical development
- Contribute to cross-functional initiatives to strengthen clinical development excellence
- Support business development activities
- Support scientific due diligence
- Support in-licensing assessments
Berufserfahrung
3 Jahre
Ausbildung
Master-Abschluss
Sprachen
Englisch – fließend
Tools & Technologien
Microsoft Office
Benefits
Kinderbetreuung
- Company day care centers
Flexibles Arbeiten
- Flexible working time
- Mobile working
Mehr Urlaubstage
- Generous annual leave
Weiterbildungsangebote
- Development discussions
- Management training courses
- Specialist training courses
- Soft skills courses
- E-learning courses
- Language courses
Mentoring & Coaching
- Coaching sessions
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens Merz Aesthetics GmbH 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.
Zur Originalanzeige bei Merz Aesthetics GmbHÜber das Unternehmen
ME
PharmaceuticalsFrankfurt am Main
Das Unternehmen ist ein unabhängiges, international tätiges Unternehmen im Bereich der ästhetischen Medizin.
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