Statistical Programmer
Current• Received extensive training on practical implementation of clinical data programming in SAS, Clinical Trial phases, GDPR, CDISC standard• Programmed and validated Non-Linear Mixed Effect Model (NONMEM), SDTM, ADaM datasets from raw source data• Write and maintain adequately documented programmes to produce statistical analysis datasets (ADS), analytical tables, listings from Statistical Analysis Plan (SAP) / Clinical Study protocol (CSP) to simulate effects of the new drug on living objects• Provide input as required at all meetings, discussions, and activities covering aspects of Statistical Programming on clinical trial level activities• Work closely with biostatisticians, data managers, and other stakeholders to understand project needs and deliverables