Job Description
Posting Title Manager, Xcellerate Monitoring Integration & configuration services
Requisition ID 68576BR
Job Category Information Technology
Locations Belgium
Belgium - Brussels
Bulgaria
Bulgaria - Sofia
Croatia
Czech Republic
Denmark
Estonia
Finland
France
Germany
Greece
Hungary
Ireland
Israel
Italy
Latvia
Lithuania
Poland
Romania
Serbia
Slovakia
Spain
Sweden
Switzerland
Ukraine
Shift 1
Job Posting The Manager is an experienced member of the Xcellerate Monitoring Integration and Configuration Services (XMICS) part of Monitoring and Data Flow Optimization Team and global risk based monitoring team and has responsibility for execution of key Risk Based Monitoring (RBM) data integration, standard and custom mapping and tool configuration and customization services and operates as a partnership level Lead XMICS Analyst. The Manager collaborates with the study team to standardize configuration plans, operational and clinical data mapping, central monitoring tools and dashboards to comply with the central monitoring configuration plans. The Manager requires working knowledge of three or more areas of programming (e.g. clinical data structures and mapping, tool configuration and JSON, JavaScript or HTML5 programming) as well as a working knowledge of broader drug development and clinical trials. He/she is responsible for overseeing accurate and timely uploading of operational and clinical trial data and refresh of central monitoring dashboards and tools. He/she provides RBM tool expertise and guidance to the study team. He/she will provide oversight of and perform some Xcellerate Monitoring, RBM and central monitoring integration and configuration services for a program of clinical studies and is responsible for line management and development of junior XMICS staff.
Education/Qualifications Recommended:
University degree education required (or experience level which may be substituted for level of education) in computational, physical or life science with a strong quantitative focus.
Experience Minimum of five years clinical trials electronic data collection (EDC) design, clinical data management, biostatistical programming OR minimum of four years hands-on experience in analysis, modeling and visualization of large complex and heterogeneous datasets.
Strong understanding of algorithms and their scalability
Strong programming skills in 3 of the following; SAS, C#, C++, R, Matlab or equivalent
Strong understanding of relational databases and SQL
Preferred:
Some experience with NoSQL databases and other big data technologies.
Some experience with web development e.g. JavaScript, JSON, Oracle InForm, Medidata Rave or HTLM5.
No experience of risk management, risk based monitoring or central monitoring is required.
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