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Senior Clinical SAS Programmer

Bengaluru, KA
Job Code:
  • Biotechnology & Science
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Job Details

ResponsibilitiesConfidently displays excellent internal and external customer serviceResponsible for implementation and execution of client statistical requirementsDemonstrates strong understanding of ICH guidelines, as applicable toclinical programmingCreates and presents programming training exercises, trains new programmers, and serves as mentorUtilizes System Development Life Cycle (SDLC) for programming deliverablesTrains via self-study and self-practice independently and explores advanced topics related to programming and/or drug developmentInteracts directly and independently with client to coordinate all facets of the project; highly competent communicator with excellent client interaction skillsProvides high level of support to the statisticians and medical writers on all programming matters according to client requirementsWorks with statisticians to provide definitions, documentation and review of derived variables needed to produce planned tables, listings, and graphsGenerates tables, listings, and graphs from clinical trial databases using SASDevelops programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related softwareDevelops data and programming specifications jointly with other programmers and biostatisticiansDesigns specific data presentations including creative summary tables, graphs, and patient listingsAssists with preparing data validation plan based on customer needsReviews data management guidelines for computer edit/validation checksIndependently implements and validates QC findings in compliance with the NC Handling ProcedureConducts thorough self-reviews of deliverables prior to release to client; serves as high level reviewer for othersDemonstrates extensive knowledge of departmental processes (e.g. competency in programming software and willingness to share information)Leads most projects with minimal management oversight, including complex projects with multiple team members and independent coordination with the clientDemonstrates excellent internal and external leadership skills for projectsComplies with Document Control ProcedureComplies with Record Control ProcedureEnsures compliance to applicable ISMS policies and proceduresJob Requirements Minimum of5 years, Work from Home option AvailableHard-core experience in Clinical Programming,Experience in CDISC Lifecycle and development of Macros. ExperienceExperience creating TLGs for Saf & Eff data, ISS, ISE, pooled studies, specs
Additional Degree: BE/ B.Tech (Engineering)

Experience: 5-10


Application Programming | Database Administration (DBA) | Quality Assurance/Testing | Software Engineer
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