Sobi
Global Product Safety Science Lead(m/w/x)
VollzeitRemoteSenior
München
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EDEdwards Lifesciences
Senior Clinical Safety Specialist(m/w/x)
München
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Tracking and processing complex adverse device events from clinical trial sites for medical device innovations. Strong medical background with cardiology experience essential. Flexible working hours, meal benefits.
Anforderungen
- Bachelor's Degree in related field
- Strong medical background, cardiology experience, and interest in clinical trial safety
- Experience in medical device, healthcare, or related environment
- Business level English (written and spoken)
- Proven expertise in MS Office Suite
- Excellent written and verbal communication skills
- Demonstrated problem-solving and critical thinking skills
- Knowledge of Edwards policies and quality compliance
- Proficient knowledge of medical terms and human anatomy
- Full knowledge of Medical Device Reporting regulations
- Good knowledge of Good Documentation Practices (GDP)
- Ability to manage confidential information with discretion
- Attention to detail
- Ability to interact professionally with all organizational levels
- Ability to manage competing priorities in a fast paced environment
- Ability to work in a team environment
- Ability to interact with senior personnel on significant matters
- Adhere to all company rules and requirements
Aufgaben
- Track and process complex adverse device events from clinical trial sites
- Collect source documents for key adverse events from clinical trial sites
- Determine regulatory reporting requirements based on event criteria and causality
- Interact with study committees for safety data collection and reconciliation
- Prepare safety event reports for clinical, regulatory, and complaint handling submissions
- Ensure compliance with worldwide reporting requirements, including expedited case reports
- Understand corporate and global regulations, guidelines, and writing practices
- Coach and mentor junior clinical safety specialists
- Handle and review adverse events according to SOP and regulatory requirements
- Identify problems and lead projects to improve processes and procedures
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office Suite
Benefits
Flexibles Arbeiten
- Flexible working hours
- Remote working
Betriebliche Altersvorsorge
- Pension plan
Sonstige Vorteile
- Risk insurance
- Service awards
Gratis oder Vergünstigte Mahlzeiten
- Meal benefits
Mehr Urlaubstage
- Enhanced leave benefits
Parkplatz & Pendelvorteile
- Transportation benefits
Attraktive Vergütung
- Employee stock purchase programme
Mentale Gesundheitsförderung
- Employee assistance programme
Gesundheits- & Fitnessangebote
- Comprehensive wellness programme
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Edwards Lifesciences 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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EDEdwards Lifesciences
Senior Clinical Safety Specialist(m/w/x)
München
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Tracking and processing complex adverse device events from clinical trial sites for medical device innovations. Strong medical background with cardiology experience essential. Flexible working hours, meal benefits.
Anforderungen
- Bachelor's Degree in related field
- Strong medical background, cardiology experience, and interest in clinical trial safety
- Experience in medical device, healthcare, or related environment
- Business level English (written and spoken)
- Proven expertise in MS Office Suite
- Excellent written and verbal communication skills
- Demonstrated problem-solving and critical thinking skills
- Knowledge of Edwards policies and quality compliance
- Proficient knowledge of medical terms and human anatomy
- Full knowledge of Medical Device Reporting regulations
- Good knowledge of Good Documentation Practices (GDP)
- Ability to manage confidential information with discretion
- Attention to detail
- Ability to interact professionally with all organizational levels
- Ability to manage competing priorities in a fast paced environment
- Ability to work in a team environment
- Ability to interact with senior personnel on significant matters
- Adhere to all company rules and requirements
Aufgaben
- Track and process complex adverse device events from clinical trial sites
- Collect source documents for key adverse events from clinical trial sites
- Determine regulatory reporting requirements based on event criteria and causality
- Interact with study committees for safety data collection and reconciliation
- Prepare safety event reports for clinical, regulatory, and complaint handling submissions
- Ensure compliance with worldwide reporting requirements, including expedited case reports
- Understand corporate and global regulations, guidelines, and writing practices
- Coach and mentor junior clinical safety specialists
- Handle and review adverse events according to SOP and regulatory requirements
- Identify problems and lead projects to improve processes and procedures
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office Suite
Benefits
Flexibles Arbeiten
- Flexible working hours
- Remote working
Betriebliche Altersvorsorge
- Pension plan
Sonstige Vorteile
- Risk insurance
- Service awards
Gratis oder Vergünstigte Mahlzeiten
- Meal benefits
Mehr Urlaubstage
- Enhanced leave benefits
Parkplatz & Pendelvorteile
- Transportation benefits
Attraktive Vergütung
- Employee stock purchase programme
Mentale Gesundheitsförderung
- Employee assistance programme
Gesundheits- & Fitnessangebote
- Comprehensive wellness programme
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Edwards Lifesciences 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
Edwards Lifesciences
Branche
Healthcare
Beschreibung
The company is a global leader in patient-focused medical innovations, offering opportunities in a dynamic work environment.
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