Beschreibung
Regulatory Affairs Data Manager (m/f/d)
Reference: -en
Start: asap
Duration: 6 MM++
Main tasks:
- Executing and provision of Data Quality reports to CSL functions (Global regulatory Affairs, GCSP), and provision of expertise for data cleansing approaches
- Management of Master data requests/new dictionaries
- Templates management
- Maintenance and update of technical system documentation
- Consultancy service for implementation of systems enhancements
- Provision of user support (e.g. status change of workflows in RIMS, provision of guidance upon user questions)
- Monthly newsletter authoring and distribution (Spotlight)
- Coordination and provision of user training/onboarding sessions for GRA-IT systems
- Optimization and maintenance of training documentation
- Facilitate user access to GRA-IT systems
Main qualifications
- High-level understanding of R&D processes with focus on Regulatory Affairs and Regulatory Information Management System
- Trackwise Digital Project Registration
- System knowledge (Sparta systems)
- Electronic Document Mgmt. D2 Live science suite (OpenText)
- English fluent
Main advantages:
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
Referencenumber:
Make contact:
Phone:
Email: