and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs Develop and validate SAS.... Candidate is a detail-oriented statistical programmer with a strong interest in clinical data analysis, regulatory processes...
. Generate, validate, and/or review tables, figures and listings to support the statistical analysis of clinical trials data... in support of regulatory submissions and publications. Generate or perform quality control for SAS programs and other study...
and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs. Develop and validate SAS.... Candidate is a detail-oriented statistical programmer with a strong interest in clinical data analysis, regulatory processes...
and SAS is helpful Strong knowledge of Good Clinical Data Management Practices, CDISC/CDASH/SDTM and other FDA and industry...Responsibilities: Leads, performs, and oversees data management activities for clinical studies and/or clinical...