Die KI-Suchmaschine für Jobs
Senior Clinical Safety Specialist(m/w/x)
Beschreibung
In this role, you will be the key Clinical Safety contact for European Clinical Trials, managing adverse events and ensuring compliance with regulatory requirements. You will collaborate with study committees and mentor junior specialists.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
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
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Senior Clinical Safety Specialist(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will be the key Clinical Safety contact for European Clinical Trials, managing adverse events and ensuring compliance with regulatory requirements. You will collaborate with study committees and mentor junior specialists.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
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
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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