Position: Sr. SAS Statistical Programmer Location: Ridgefield Park, NJ
Duration: 9+ months Must be local *Description: * Provide statistical programming and validation support for clinical studies, including overseeing and validating programming activities by external vendors (e.g., CROs) · Provide programming supports for publication and marketing strategies, work closely with manager of programming to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies. Work with the clinical study team on study design, development and/or review of clinical study protocols, statistical analysis plans and final study report; perform post-hoc statistical analyses as needed. · May work with the Health Outcome team on the design/analysis/validation of projects. Develop dataset specifications, provide input to database and CRF development, create edit check programs and listing generation macros for Data Management. *Qualifications: * At lest 5 years experience in SAS programming for Phase I-IV clinical trials in pharmaceutical/CRO environment. Bachelor's degree in Statistics or a related science discipline (Master or PhD in Statistics preferred). Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS office. Experience with Unix and Windows operating systems. Understanding FDA guidelines. Some experience in CDASH and SDTM is a plus. Thanks & Regards Alex Technical Recruiter Phone No.: 605-741-0116 Email ID: [email protected] Website: www.nexgenb.com
