Masters in Pharma, Regulatory affairs, Life Sciences, Statistics, biostatistics or related+1 year experience.
Build programs to create SAS datasets from the clinical database, external data sources, and other sources while following the clinical study's protocol or statistical plans.
Required experience in SAS Code, GDMP and regulatory compliance in accordance with US FDA, Maintaining SAS data in accordance with CDISC standards.
KRL Solutions
Las Vegas, NV