40211 Düsseldorf
Vollzeit
15.01.2025
Vollzeit
Stellenbeschreibung
Job Profile:
- Generation of essential study documents like data management plan and data validation plan
- Set-up of clinical study data bases and validation
- Programming of consistency and plausibility checks
- Development of paper and eCRF
- Validation of programs, data base audits
- Generation of CDISC/SDTM files
- Participation in the development and implementation of data management processes
Requirements:
- University degree (PhD/MSc) in Mathematics, Statistics or Natural Science or certified in medical documentation
- Comprehensive knowledge of data management in clinical studies
- Practical experience with data management in clinical studies
- Practical experience with CDISC
- Comprehensive knowledge in SAS
- Self-motivated, good communicator and team player.
