Description
I have an exciting project to work for a large organisation in Dubai.
Your Accountabilities/Responsibilities:
Provide advanced level of SAS programming activities for the monitoring
Collaborate with project biostatistician in the creation, implementation, and maintenance of execution plan accounting for timeline, resource and quality of the projects
- Ensures that all statistical programs comply with the programming coding standards and utilize available standard reporting systems, as well as macro utility programs.
- Support statistical programming applications that are used to generate clinical study reports.
- Support ADS and TLG generation, and assist with the development of work flow and SOPs for Biostatistics and Statistical Programming operations.
- Accountable for the provision of standard and non-standard data sets, tables, listings and figures based on the final synopsis and SAP that are required for the study reports, submissions and product defense.
- Communicates effectively not only within the teams and functional lines but also with the external resources
- Provides filing, approval and regulatory programming support for all aspects of a submission
Your Qualifications:
Degree in life sciences, statistics, biostatistics, or equivalent areas with extensive experience in pharmaceutical industry, medicine or a relevant field is preferred.
Extensive SAS programming skills (5 Years)
Knowledge of base SAS, SAS macro language, graph, FSP, STATS, SQL as well as other programming languages.
Must have Pharmaceutical Experience (CRO/Pharma/Biotech)
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