Referenznummer: 424540/1 Startdatum: asap Projektdauer: 24 MM Ort: Hessen
Define the data collection for clinical studies by creating data definitions in the metadata repository and by using programmatic tools
Create eCRFs in the Medidata Rave EDC systems by implementing defined data collection standards into the study and amend it with study specific customizations and additions
Support the definition of metadata for non-eCRF data sources in the metadata repository system to allow automated processing of incoming and outgoing data for all data sources used in clinical studies
Support the mapping of data collected in eCRFs or eCOA tools into standardized formats following the CDISC standard to enable standardization and data pooling
Profound experience in either clinical data management and/or statistical programming, within the CRO/pharmaceutical environment
Understanding of data management and/or statistical programming processes and standards including standards metadata management
Strong knowledge in CDISC standards (CDASH, SDTM, ADaM)
Good SAS programming skills
Strong Medidata Rave knowledge in study build, edit check programming
Good understanding of the Medidata Rave Core Configuration and Lab Administration
A highly motivated team and an open way of communication
Über Hays: 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.
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