evelop statistical programs using SAS to analyze clinical/non-clinical trial data; Assess data accuracy and consistency, identify protocol violations, implement statistical analyses, design and develop analysis files and produce TFL; Participate in the development of case report forms and quality control specifications; Use and improve company SAS macros.Experience: Two years of working experience, preferable in SAS programming. Competencies: Ability to learn, team work, quality orientation, effective communication.| 欢迎光临 数学建模社区-数学中国 (http://www.madio.net/) | Powered by Discuz! X2.5 |