Core Competencies Required:
Review protocols, CRFs, annotated CRFs, test databases and Statistical Analysis Plans Provide statistical programming support to team primarily using SAS software: Develop, test and produce derived datasets, tables, listings and graphs for clinical study reports. Validate derived datasets, tables, listings and graphs for clinical study reports. Importing and exporting data files Extraction of data from database (e.g. Clintrial) Assist with Quality Control Activities Assist with development of departmental guidelines in line with the standardization of programs and systems for the generation of CSR components Generate and maintain study documentation Attend and participate in project team meetings
Bachelors degree in Statistics, Computer Science, Mathematics or related discipline.
Good SAS programming skills with 5to 7 years experience in the pharmaceutical industry or a clinical research organization. Skills should include Base SAS, SAS Macro and SAS ODS. Basic understanding of Software Development Lifecycle. Good verbal and written communication skills. Ability to work on multiple projects, plan, organize and prioritize activities