Clinical Affairs & Quality Management Specialist m/f/d

Full or part time

Your tasks:

• Management, monitoring and supervision of preclinical and clinical study projects
• Contract management of study projects
• Registration of clinical studies with the competent authority
• Maintaining and developing the QM system
• Development of strategies for clinical evidence
• Preparation of reports and presentations of study results

Your profile:

• Successfully completed technical studies, ideally quality management or medical technology
• 2 years professional experience in the field of quality management / clinical affairs, ideally in medical technology
• German and English business fluent

Desirable:

• Qualification as an auditor
• Knowledge Quality Management (DIN EN ISO 13485) and / or Regulatory Affairs

Your advantages:

• Collaboration in an active and synergetic team with a pleasant communication culture
• Attractive base salary with variable remuneration components
• Growth location with high quality of life in the tri-border region
• Corporate Health Management

We look forward to your electronic application (pdf format), quoting references, your salary expectations and notice period, to: careers@cortec-neuro.com. Your contact person is Ina Saumer.

Please Apply here.