Beschreibung
We are looking for a
Global Clinical Monitoring Process and Compliance Specialist (m/f)
Referenz: -en
Beginn: asap
Dauer: 13 MM++
Ort: in Basel region
Branche: Herstellung von pharmazeutischen Erzeugnissen
Ihre Aufgaben:
- Process improvements in global clinical monitoring
- Create and Update Q- documents
- Track and follow Audit CAPAs for Global Clinical Monitoring
- Ensure compliance
- Improve processes
Ihre Qualifikation
- Very good know-how in clinical trials, especially in monitoring and project management
- Deep knowledge of processes in clinical monitoring and its related areas
- Excellent communication skills
- English spoken and written
Skills:
- Clinical development manager
Keywords: Clinical Development Manager Compliance Clinical Trials Process improvement Audit CAPAs