Merz Therapeutics
Regional Regulatory Affairs Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Frankfurt am Main
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OTOtsuka Pharma GmbH
Associate Director Global Regulatory Affairs(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Global regulatory strategy development for investigational and marketed drugs. Comprehensive drug development, laws, and global regulations knowledge required. Document creation for submission and approval.
Anforderungen
- Comprehensive drug development process knowledge
- Comprehensive drug laws knowledge
- Comprehensive global regulations knowledge
- Comprehensive guidelines knowledge
- Good understanding of global regulatory agencies
- Leading CTA submission experience
- Leading IND submission experience
- Leading sNDA/NDA/MAA/Variations submission experience
- University degree in Medicine, Pharmacy, Life Sciences or Chemistry
- Several years clinical/industry/health authority experience
- Preferably global or European role experience
- Good CMC knowledge
- Experience in Oncology therapeutic field
- Experience in CNS therapeutic field
- Experience in Cardio-Renal therapeutic field
- Strong information searching skills
- Strong summarization skills
- Strong assessment skills
- Microsoft Word proficiency
- Microsoft Excel proficiency
- Microsoft PowerPoint proficiency
- Microsoft Outlook proficiency
- Strong analytical skills
- Problem solving ability
- Strong communication skills
- Strong presentation skills
- Excellent English language command
- Experience in cross-functional project teams
- Experience in multi-cultural project teams
- Communicating with cross-functional project teams
- Communicating with multi-cultural project teams
- Involving internal and external experts
- Strong knowledge in European Regulatory Affairs
- Experience in European Regulatory Affairs
- Strategic European Regulatory Affairs aspects
- Operational European Regulatory Affairs aspects
Aufgaben
- Provide global regulatory expertise for pre-clinical, clinical, and commercial areas
- Ensure regulatory and competitive intelligence is searched, summarized, and disseminated
- Collaborate with Regulatory Management to establish clear regulatory pathways
- Create accurate and timely documents for submission and final approval
- Develop global regulatory strategy and plan for investigational and marketed drugs
- Manage lifecycle regulatory activities in alignment with Therapeutic Area Lead
- Serve as primary contact to Competent Authorities in Europe and other regions
- Identify and obtain regulatory intelligence and precedent approvals
- Translate complex global requirements and assess regulatory challenges
- Lead cross-functional teams to develop global regulatory plans and address issues
- Respond to health authority queries and meet regulatory obligations
- Develop and lead strategy for Health Authority interactions and communications
- Review submission documents for alignment with strategic approach
- Design programs for complete and accurate IND/CTA/NDA/MAA submissions
- Ensure clinical trials meet regulatory requirements
- Support development of strategies and review responses for health authority submissions
- Review submission documents for consistency and strategic alignment
- Interact with regulatory agencies and document conversations
- Contribute to product registration, progress reports, and adverse experience reports
- Collaborate with outsourced suppliers for regulatory document preparation
- Identify and communicate major regulatory issues to stakeholders
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Microsoft Outlook
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Otsuka Pharma 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.
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OTOtsuka Pharma GmbH
Associate Director Global Regulatory Affairs(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Global regulatory strategy development for investigational and marketed drugs. Comprehensive drug development, laws, and global regulations knowledge required. Document creation for submission and approval.
Anforderungen
- Comprehensive drug development process knowledge
- Comprehensive drug laws knowledge
- Comprehensive global regulations knowledge
- Comprehensive guidelines knowledge
- Good understanding of global regulatory agencies
- Leading CTA submission experience
- Leading IND submission experience
- Leading sNDA/NDA/MAA/Variations submission experience
- University degree in Medicine, Pharmacy, Life Sciences or Chemistry
- Several years clinical/industry/health authority experience
- Preferably global or European role experience
- Good CMC knowledge
- Experience in Oncology therapeutic field
- Experience in CNS therapeutic field
- Experience in Cardio-Renal therapeutic field
- Strong information searching skills
- Strong summarization skills
- Strong assessment skills
- Microsoft Word proficiency
- Microsoft Excel proficiency
- Microsoft PowerPoint proficiency
- Microsoft Outlook proficiency
- Strong analytical skills
- Problem solving ability
- Strong communication skills
- Strong presentation skills
- Excellent English language command
- Experience in cross-functional project teams
- Experience in multi-cultural project teams
- Communicating with cross-functional project teams
- Communicating with multi-cultural project teams
- Involving internal and external experts
- Strong knowledge in European Regulatory Affairs
- Experience in European Regulatory Affairs
- Strategic European Regulatory Affairs aspects
- Operational European Regulatory Affairs aspects
Aufgaben
- Provide global regulatory expertise for pre-clinical, clinical, and commercial areas
- Ensure regulatory and competitive intelligence is searched, summarized, and disseminated
- Collaborate with Regulatory Management to establish clear regulatory pathways
- Create accurate and timely documents for submission and final approval
- Develop global regulatory strategy and plan for investigational and marketed drugs
- Manage lifecycle regulatory activities in alignment with Therapeutic Area Lead
- Serve as primary contact to Competent Authorities in Europe and other regions
- Identify and obtain regulatory intelligence and precedent approvals
- Translate complex global requirements and assess regulatory challenges
- Lead cross-functional teams to develop global regulatory plans and address issues
- Respond to health authority queries and meet regulatory obligations
- Develop and lead strategy for Health Authority interactions and communications
- Review submission documents for alignment with strategic approach
- Design programs for complete and accurate IND/CTA/NDA/MAA submissions
- Ensure clinical trials meet regulatory requirements
- Support development of strategies and review responses for health authority submissions
- Review submission documents for consistency and strategic alignment
- Interact with regulatory agencies and document conversations
- Contribute to product registration, progress reports, and adverse experience reports
- Collaborate with outsourced suppliers for regulatory document preparation
- Identify and communicate major regulatory issues to stakeholders
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Microsoft Outlook
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Otsuka Pharma 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.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Otsuka Pharma GmbH
Branche
Pharmaceuticals
Beschreibung
Otsuka Pharma GmbH ist ein Unternehmen, das sich auf pharmazeutische Produkte spezialisiert hat.
Noch nicht perfekt?
- Merz Therapeutics
Regional Regulatory Affairs Manager(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - Lilly Deutschland GmbH
Associate Director - Patient Safety and Regulatory Affairs(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBad Homburg vor der Höhe - Merz Therapeutics
Team Lead Regulatory Affairs Regions(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Regulatory Site Officer(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
Study Start Up Associate II(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main