Senior Clinical Programmer

 statistical outputs from studies Lead statistical programming activities on studies and deliverables, and assist management and biostatisticians with complex projects Required Qualifications Minimum of a Bachelor's Degree in Statistics, Mathematical Science, Physics, or a Computing related field Minimum 3 years of hands-on statistical programming experience in a CRO or pharmaceutical clinical trials environment Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, and SAS/ODS Experience applying CDISC requirements to generate ADaM datasets and supporting documentation Familiarity with Pinnacle 21 validation and experience in early-phase clinical trials