Global Clinical Safety and Pharmacovigilance Process Specialist (f/m/d)

Overview:
• Start date: ASAP
• Time of contract: 8 months
• Working hours per week: 40
• Location (on site or remote): Mainly remote
• Language requirements: English, German

Main responsibilities:
• Support with content development for Regions SharePoints and
dashboards
• Support with global and local procedural documents incl. flowcharts for
Regions and Safety Officer (developing new documents, updating
documents)
• Act as interface to platform & tools developers, coordinate development
and enhancements of process platforms
• Support with user requirements and test scripts for tools validation
• Support the development of global and local standards for Regions Team
& Safety Officers
• Closely collaborate with Regions Team members, Safety officers and
Regions interfaces
• Support creation of Regions Process landscape in MS Visio & ARIS
• Support of content development (PV) and technical maintenance for
Regions PV Education platform (MS SharePoint)
• Support User Interface Design of Regions tools and platforms
• Support development & implementation of processes standardization
• Support with coordination and follow-up of data maintenance processed
by Safety Officers

Experience:
• Technical skills in MS SharePoint, Power BI, Power Apps, ARIS, Visio
• Experience in PV business process development and standards
• Understanding of platform/project management and process
improvement
• If possible, experience in the Pharmaceutical or Biotech industry
• If possible, experience in writing procedural documents