Dear Allstat,
Please find below our latest permanent role:-
Senior Clinical Programmer
Permanent
Global Pharma
Based in Netherlands (100% Client site)
Excellent salary and package
Key responsibilities:
- In this role you will be responsible for advising study teams, creating databases and implementing, validating and maintaining all data collection instruments required in clinical studies. In order to achieve these goals you will focus primarily on
- Designing and building databases for clinical studies according to local and global standards by applying your knowledge of database design standards and the Clinical Data Management System
- Providing expertise to the R&D Organization by advising study teams in all database and data collection related matters
- Setting up Electronic Data Capture (EDC) for individual clinical studies
- Working in close collaboration with the study teams and data management, and coordinating with colleagues in other regions and at outside vendors
Minimum requirements
- Masters degree in life science or computing science
- Good programming skills (SQL). Experience with database setup is required; experience with EDC is an advantage
- Basic understanding of relational database structures
- Over 3 year experience within the pharmaceutical industry either as Database Manager or Data Manager
- Must have MEDIDATA Rave
For a confidential consultation call Laura Christie on +44 207 633 4825 or email your CV to [log in to unmask]
I look forward to hearing from you.
Kind regards,
Laura
Laura Christie
Principal Consultant, Biometrics, Europe
Recruiting experts in Pharma
HAYS Recruiting experts worldwide
25-27 Wootton Street
London
SE1 8TG
T: +44 207 633 4825
M: +44 7900 932031
F: +44 207 922 7101
E: [log in to unmask]<mailto:[log in to unmask]>
hayspharma.com
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