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Senior SAS programmer Desio Italy,  

Posted on : 08 March 2017

Project Description

Location Desio (MB), Italy Job Description JOB DESCRIPTION The Senior SAS Programmer, under the supervision of the Scientific Director, is in charge of the following activities: Develop SAS programs for generating datasets, tables, figures and listings for clinical trials (according to ICH E3) and/or publication and/or Health Authorities requests Be the CDISC SDTM/ADaM expert; use CDISC guidelines to generate SDTM/ADaM datasets Develop standard SAS macros and prepare the corresponding validation documents Perform quality check on SAS programs/outputs created by another Statistician/SAS Programmer Develop SAS programs/macros and utilities for data cleaning Liaise with Data Management team in identifying and implementing checks according to the Data Validation Plan Check the requirements to handle external clinical data and develop the SAS programs to import/reconcile external clinical data Develop and validate SAS programs for identification of Protocol Deviations Establish and implement programming rules Collaborate with Biostatistics and Data Management staff on clinical trials/projects Prepare, maintain, and archive of SAS programming documentation Collaborate in establishing and maintaining SOPs related to SAS programming Collaborate in establishing and maintaining document/programming standards Contribute to on-boarding of new associates and act as a mentor for junior staff Keep informed on new SAS developments relevant to the clinical trial data management JOB REQUIREMENTS Scientifical Degree, preferably in Statistics Excellent knowledge of SAS programming and associated features and their applications Excellent knowledge of CDISC Excellent spoken and written English required Good team player with good communication skills Thorough understanding of relational database and theory Good at generating new ideas and solutions


Desio (MB) Italy

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