|Over eight years of experience in SAS programming for Phase I-IV and non-interventional clinical trials. Development and QC of SAS programs to create listings and reports. Programming and QC of data sets according to CDISC SDTM guidelines.||Over ten years of experience in clinical data management of Phase I-IV and non-interventional clinical trials. Lead data manager for six studies. CRF preparation based on CDISC/ODM standards. Full data cleaning/query management. Standardized data according to CDISC SDTM format.|
Develop and program data listings, custom reports and data sets for both internal and sponsor use. Perform quality control programming of clinical data management and statistical programs. Provide technical expertise and guidance to lower level programmers and data management personnel. Program and programming QC of:
Reviewed CRFs for data entry. Identified and resolved data discrepancies for phase II and III US and European clinical trials. Developed and wrote edit checks.
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