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Irfa******
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Italy
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Last Update: 08.01.2019 at 12:00
Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Verona Area, Italy
Country
Italy
Category
Regulatory, Quality and Clinical
Description
Primary Responsibilities
Programming of datasets according to CDISC SEND, SDTM and ADaM guidelines
Accountable for all tasks related to the statistical programming: Production of TFL, validation/QC of SAS Programs, creating macros for pharmaceutical development and drug discovery analysis
Meet deadlines and deliver high quality work
Regular report presentation in meetings and frequent communication with internal project team members and external clients references
Required skills or attributes
Bachelor or Master in Statistics, Computer Science or relevant field is desirable
Good understanding of pharmaceutical Research