programming. Requirements: Minimum of 5 years of experience in developing software for clinical trials using the SAS system... documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinical study...
experience in statistical programming with clinical trial data, particularly using SAS software. A strong team player who...
. Generate, validate, and/or review tables, figures and listings to support the statistical analysis of clinical trials data... in support of regulatory submissions and publications Generate or perform quality control for SAS programs and other study...
Join a sponsor-dedicated team, progressing with in-house study activities over the years. Experienced R programmer... needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software...
Join a sponsor-dedicated team, progressing with in-house study activities over the years. Experienced R programmer... needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software...
collaboratively with Clinical Operation, Data Management,Global Drug Safety, Regulatory and Project Management management/staff... years of clinical trial programming experience in the biotechnology, pharmaceutical or health related industry. Advanced...