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Senior Statistical Programmer

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

Deliver best value and high quality service Ability to fill Statistical Programming Coordinator role on projects. The Statistical ProgrammingCoordinator willo Input into and negotiate statistical programming timelines. Ensure that timelines areadhered to.o Coordinate and lead a statistical programming team to successful completion of a studywithin given timelines and budgeto Monitor project resourcing, project budgets, and identify changes in scope Interact with Sponsors as the key contact with regard to statistical programming issues Provide technical support and advice to the internal team Check own work in an ongoing way to ensure first-time quality Ensure quality control (QC) on all process and technical activities related to derived dataset, table, listing, and figure programming in accordance with corporate quality standards, WSOPs/Guidelines, ICH-GCP and/or other international regulatory requirements are performed.Coordinate project start-up activities, including Unix/PMED project area set-up, creation of globalprograms (e.g.,,, etc.), tracking spreadsheets, and required documentation. Assist in the production and QC of analysis plans, produce and QC TLF mock-shells, derived dataset specifications, programming specifications, and other process supporting documents. Use efficient programming techniques to produce and/or QC derived datasets tables, figures and data listings. Understand regulatory requirements concerning industry technical standards (e.g., CDISC, 21 CFRPart 11, electronic submissions, etc.) and implications for the department. Provide input into monthly PERFORM forecasts and monitor the completion of forecasted units. Create standard macros and applications to improve the efficiency of the department. Maintain all supporting documentation for studies in accordance with WSOPs/Guidelines toensure traceability and regulatory compliance Be trained in sponsor WSOPs and disseminate knowledge to project team members asappropriate. Proactively participate in and/or lead process/quality improvement initiatives Work closely with the Quality Management Groups (QMG) to ensure compliance withWSOPs/Guidelines, ICH-GCP and any other applicable local and international regulations andparticipate in internal/external audits and regulatory inspections as required Develop wider knowledge of SAS and other relevant programming languages and processeswithin the GRO, Biostatistics, and Medical arenas. Maintain and expand local and international regulatory knowledge within the clinical industry Assist project teams in the resolution of problems encountered in the conduct of their daily work Provide relevant training and mentorship to staff and project teams
Additional Degree: BA (Arts) | B.Com. (Commerce) | B.Pharm. (Pharmacy) | B.Plan. (Planning) | B.Sc. (Science) | BBA/ BBM/ BBS | BCA (Computer Application) | Diploma-Other Diploma | B.Ed. (Education) | BHM (Hotel Management)

Experience: 3-8


Data Management/ Statistics
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