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Statistical Programmer Health Science/Pharma Molecular Connections

3.0 - 7.0 years

0 Lacs

karnataka

On-site

You will be a valued member of our clinical research team as a Statistical Programmer, where your primary responsibility will be to program, validate, and deliver statistical outputs for clinical trials. In this role, you will play a crucial part in ensuring compliance with regulatory standards and industry best practices. Your key responsibilities will include developing and maintaining SAS programs for clinical trial data processing, analysis, and reporting. You will be required to map clinical trial data to CDISC standards (SDTM and ADaM) to ensure compliance with regulatory requirements. Creating and maintaining analysis datasets following CDISC implementation guidelines will also be a p...

Posted 3 months ago

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