Additionally, you will contribute by:
- performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming;
- applying your CDISC know-how and proficiency in SDTM and ADaM, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s);
- generating complex ad-hoc reports
- preparing and validating submission packages, i.e. define.xml, Reviewers Guide
- applying your strong understanding/experience with Efficacy analysis;
- preparing submission packages
- performing lead duties when called upon;
- serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;
- being adaptable and flexible when priorities change