Informationen

Gebiet: München und Remote

Indikationen: Medizinprodukte

Job ID: 19186

Beschreibung

For our location in Munic we are looking for an:


Global Medical Affairs Manager (f/m/d)

                                                                           
Your Role

  • Serve as the medical and device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, complaints, voice of the customer, and voice of the business.
  • Devise novel approaches to address clinical and technical problems in clinical practice through development and modification of related medical devices.
  • Provide accurate, balanced, and timely clinical expertise to functional areas such as clinical development, R&D, marketing, manufacturing, quality assurance, regulatory affairs, and legal based on objective evidence, clinical experience, and voice of the customer.
  • Assimilate voice of customer and clinical experience for design input with new product development and product lifecycle management.
  • Provide clinical expertise for creation and development of risk assessments and quality standards for product design history files.
  • Develop and deliver relevant medical device training programs (e.g. written, verbal, and eLearning) that support product implementation, training, and marketing efforts.
  • Train internal customers on product application, disease states, and regional differences as required.
  • Support product implementation process creation, maintenance, and controlled launch when applicable.
  • Maintain familiarity of published literature as objective evidence for clinical trends and therapies related to impact on product lines.
  • willing to travel (50%)


                                
Qualification

  • Degree in related clinical discipline (Advanced Practice Degree preferred, Master’s level or higher) or equivalent relevant experience required.
  • Critical Care, Medical Surgical, Surgical Experience
  • Minimum 5 years of related clinical experience required
  • Active license in the territory in good standing required with clinical expertise.
  • Excellent written, oral communication, and organizational skills.
  • Effective and competent presentation and teaching skills.
  • Self-motivated, independent, multi-tasking, team-oriented individual with exceptional follow through.
  • Upstream Medical Affairs R&D experience
  • Able to communicate complex scientific/clinical issues in a concise and clear manner.
  • Has executive presence and ability to influence customers and other stakeholders.
  • Broad understanding of the regulatory and healthcare environment (MDR), particularly in Eastern Europe.
  • Empathetic style with the ability to motivate others.
  • Proven experience and success working in highly matrixed organizations.
  • Language skills: fluency in German and English
                              

                                                                                
                                                                                  
Contact Details
                                                                           
Bei Fragen erreichen Sie Katharina Hartecker unter der Telefonnummer: 0621-7502202

Interne Kennziffer: 19186

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