Clinical Statistical Programmer

Clinical Statistical Programmer #statistical #inferentialstatistics #statisticians #statistics #stat #probability #statisticsandprobability #statslove #statlove #mathematics #inferential #statistic #statsforlife #biostatisticians #statsforlifee #estimation #significance #inference #nonparametric #parametric #datascience #bigdata #analytics #interpretation #testing Job Title : Clinical Statistical Programmer Job location : Chennai Bangalore Home based Office based No of years of experience: 3+ years of relevant exp in SDTM domain and SAS Skills Education Qualification: Any graduation Salary : As per Industry standards with attractive benefits Skill set : Strong knowledge of SAS programming language, Define.xml, SDTM aCRF, cSDRGs Job Functions: Responsible for the integrity of the programmingcomputing solutions for multiple clinical trials or equivalent andor publication activities. In collaboration with the Biostatistician and Senior Programmer, provide programming support to projectlevel programming deliverables and other adhoc programming requests. Ensure understanding and compliance with study and project programming standards. Responsible for development of programming specification. Support the full execution of final production run and programming activities for a project or an indication with guidance from senior team members. Maintain optimum communication with internal and external study team members, Lead Programmer and Lead Statistician and provide status of programming activities as and when required. Maintain uptodate, accurate progress of the assigned programming deliverables and ensure high efficiency and timely completion according to agreed timelines, report to Lead Programmer andor Lead Statistician in case of any potential challenges. Ensure quality deliverables and compliance with validation process for audit readiness. Provide support for audit preparation as required. Ensure awareness of other programming responsibilities like creation of programming summary report, CRF review, Case Report Tabulations, CRF annotation and should be ready to provide inputs if required. Under minimal mentorship participate in establishing working relationship on assigned studies with external service provider according to agreed contract and internal business guidance. Provide input on process improvement initiatives and participate in nonclinical project activities.