Job Description Statistical Programmer with expertise in SDTMs, ADaMs & TFLs, and experience in Regulatory Submissions. End-to-end programming from CRF collections through Regulatory submission. Review eCRF, discuss data structures and participate in data review activities. Provide input into statistical programming solutions and/or ensure their efficient implementation. Maintain up-to-date knowledge of programming software (e.g. SAS) as well as industry requirements (e.g. CDISC SDTM/ADaM, eCTD, Define.xml), attend functional meetings and trainings. Contributes to assigned parts of process improvement, standardization and other non-clinical initiatives. Creation of mock shells of TLGs As assigned, act as subject matter expert (SME) or contribute to process improvement/non-clinical project initiatives with a focus on programming and analysis reporting procedures.
Interested candidates are required to send their resume to: am******************1@gm**l.com
