Sr Statistical Programmer

• Responsible for designing, developing, validating and documenting SAS programs to generate data listings for data review, create raw datasets and analysis datasets, analyze data; generate summary tables, figures and
• Maintain up-to-date knowledge of programming software ( SAS) as well as industry requirements ( CDISC SDTM/ADaM, eCTD, ), attend functional meetings and training
• Responsible for assisting statisticians in the development and review of Statistical Analysis plans and programming specifications
• Responsible for assisting data management with implementing protocols and support of annotated Case Report Forms (CRFs), database creation, coding configuration, edit check
• Review the eCRF, data structures and data review Comply with company, department and industry standards ( CDISC) and processes, create/support the review of programming specifications as part of the analysis plans
• Responsible for assisting data management in the development and programming of edit
• Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings,
• Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis

• Preferred - Btech/BE in CSE or Mtech/ME in CSE, BSc/MSc in Computer Science or BCA/MCA or BSc/Msc in Statistics
• Minimum 3 6 years of experience (CDISC, SDTM, Adam, Safety Tables TLFs and Clinical Trials ll-lV phases) within CRO / BioTech
• The ability to deal effectively with sponsors and internal customers at all
• Excellent communication and interpersonal skills, both written and

Skills : cdisc,sdtm,tlf,safety tables,clinica trials ll-lv pharses