Clinical Research
vor 2 Wochen
- Your main tasks:
- Collaboration in Medical Affairs Team projects for product development and maintenance
- Planning of clinical documentation for approval and clinical risk management
- Function as Study Manager responsible for managing clinical projects
- Developing and implementing global clinical research projects
- Building relationships with local & international opinion leaders
- Supporting R&D, Marketing & Sales through medical-scientific activities
- Conducting training & education activities internally and externally
- Creating and updating Clinical Evaluation Reports, PMCF Plan/Reports
- Preparing clinical development plans for new products and indications
- Conducting literature research and evaluations related to products and therapeutic areas
- Ensuring GCP-compliant documentation for clinical trials
- Creating and revising training material for Medical Affairs and other departments
- Addressing medical issues and intervening in cases of non-compliance
Your profile:
- MSc degree in a natural science or health field, or equivalent
- PhD or Dr. degree is advantageous
- Over 2 years of experience in clinical trial planning and monitoring
- Experience in clinical evaluation of medical devices
- Good knowledge of standard requirements ISO 14155-GCP, MEDDEV 2.7.1 rev.4, and 2017/745 for Medical Devices (MDR)
- Sound understanding of clinical research/testing methodology
- Fluency in written and spoken English, knowledge of other languages is a plus
Opportunities:
You will have the chance to work on interesting projects, grow professionally, and enjoy attractive employment conditions. Join us in shaping the innovative world of medical technology Submit your application online with details on availability and salary expectations.
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