RDEA_42508
Clinical Quality & Evaluation Specialist (m/f/d) Clinical Research
Innsbruck, Austria
Professionals
Full-Time 38.5h
Permanent
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Your Tasks
Maintenance of the Clinical Research Team’s quality management system, including the creation and updating of SOPs, CTQM, and relevant CIOMs in compliance with regulatory requirements and company policies
Organization of regulatory trainings for internal and external partners
Submission and ongoing updating of clinical study information in WHO databases and on clinicaltrials.gov
Coordination of quality event documentation, including CAPA actions, and support during audits and inspections
Ensuring the flow of clinical evidence from research to clinical evaluation; primary point of contact for Regulatory Affairs (RA) and Quality Assurance (QA) during audits and inspections
Your Profile
Bachelor’s degree or higher degree (University, FH) or its international equivalent in clinical, science, or health-related field from an accredited institution
Good knowledge of regulatory requirements in medical technology
Experience with MS Office, review tools, reference management, and document management is an advantage
Excellent German and English skills, both written and spoken
Your Benefits
Central Location
Employee Discounts
Flexible Hours
International Environment
Onboarding
Workplace Well-Being
Further information
Minimum Salary
Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is € 46,781.00.
Earliest Entry Date
This position is to be filled immediately.
Your Contact Person
If you have any questions please contact Marina Engl.
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MED-EL Medical Electronics
Fürstenweg 77a | 6020 Innsbruck, Austria | office@medel.com
medel.com