Die KI-Suchmaschine für Jobs
Senior Clinical Affairs Specialist(m/w/x)
Beschreibung
As a technical expert in Freiburg, you will lead the clinical evaluation process for innovative medical devices, ensuring product safety and regulatory compliance throughout their entire lifecycle.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree in life sciences, medical engineering, or equivalent
- •Several years of clinical or academic research experience
- •Proven medical or scientific writing experience
- •Experience in data analysis and statistics
- •Experience in a regulated environment preferred
- •Knowledge of Clinical Evaluation regulations preferred
- •Experience with clinical study design and analysis
- •Independent work, decision-making, and project leadership
- •Excellent communication and stakeholder-management skills
- •Strong analytical mindset for scientific data
- •Proactive, collaborative, and international teamwork skills
- •Full professional English proficiency and German fluency
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Lead the clinical evaluation process
- •Develop and update CEP, CER, SSCP, and PMCF deliverables
- •Perform complex literature reviews and analyze medical trends
- •Develop sustainable literature search strategies
- •Manage clinical evidence strategies during product development
- •Align clinical goals with marketing and regulatory strategies
- •Define and defend clinical strategies for international approvals
- •Support new product development and post-market surveillance
- •Provide expert clinical guidance to cross-functional teams
- •Refine clinical evaluation methodologies to meet evolving regulations
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – verhandlungssicher
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Senior Clinical Affairs Specialist(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
As a technical expert in Freiburg, you will lead the clinical evaluation process for innovative medical devices, ensuring product safety and regulatory compliance throughout their entire lifecycle.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree in life sciences, medical engineering, or equivalent
- •Several years of clinical or academic research experience
- •Proven medical or scientific writing experience
- •Experience in data analysis and statistics
- •Experience in a regulated environment preferred
- •Knowledge of Clinical Evaluation regulations preferred
- •Experience with clinical study design and analysis
- •Independent work, decision-making, and project leadership
- •Excellent communication and stakeholder-management skills
- •Strong analytical mindset for scientific data
- •Proactive, collaborative, and international teamwork skills
- •Full professional English proficiency and German fluency
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Lead the clinical evaluation process
- •Develop and update CEP, CER, SSCP, and PMCF deliverables
- •Perform complex literature reviews and analyze medical trends
- •Develop sustainable literature search strategies
- •Manage clinical evidence strategies during product development
- •Align clinical goals with marketing and regulatory strategies
- •Define and defend clinical strategies for international approvals
- •Support new product development and post-market surveillance
- •Provide expert clinical guidance to cross-functional teams
- •Refine clinical evaluation methodologies to meet evolving regulations
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – verhandlungssicher
Über das Unternehmen
Stryker
Branche
Healthcare
Beschreibung
Das Unternehmen ist ein globales Medizintechnikunternehmen, das hochwertige Implantate für den Bereich Trauma & Extremities fertigt.
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