Description
Accountable for developing software code and associated life cycle deliverables for PC and Mainframe applications. Interprets process, data modules, and business requirements into software code. Analyzes, designs, develops, implements and maintains moderate to complex computer programs and subsystems. Performs all of the steps required to design, test, and code such programs. Develops procedures and operating instructions, and successfully moves programs into production. Provides production support through problems analysis and resolution to correct deficiencies. Performs assignments under direct supervision.SKILLS:
Requirements:
- 8 years SAS pharmaceutical/biotech statistical programming experience, both efficacy and safety programming
- Bachelor's degree in Computer Science or Business Administration or equivalent training or work experience.
- Minimum of two years as a software developer.
- Oncology experience
- Onsite required
- Macro writing experience
- CDISC experience helpful but not required.
Analyze problem or new request; design problem or new request resolution; familiar with SDLC methodologies; develop program specifications; design testing requirements; code modules according to specifications and client standards; prepare test plan and test modules; develop program and system documentation; conduct program and system implementation; maintain application production environment; respond and resolve production problems; and respond and resolve user inquiries.