Duties: Design & develop software modules for the Clinical Trial Information Management Suite (CIMS). Gather requirements and specifications from users and clients. Perform web services & database programming. Prepare development plans & related technical documentation.Perform technical support, system testing and create test reports. Provide technical training and presentations.
STATISTICAL PROGRAMMERS (ANALYSTS)
Duties: Perform statistical analysis, programming and validation on clinical data. Summarize data and prepare reports with graphical illustrations on trial results. Verify data and assist in statistical modeling using statistical software. Participate in related project meetings. Participate in study design, sample size estimate, protocol writing and statistical analysis plan (SAP). Present and interpret study results to clients.
Requirements: Masters degree in statistics or closely-related field; ability to perform SAS programming, in-depth statistical analysis and modeling. Multiple openings.