Statistical Programmer

Hands on programming role, supporting deliverables in the study/project/portfolio/standards team, of less or medium complex statistical programming deliverables - Mentored/Guided by Senior Statistical Programmers within Standards/Study/Project/Portfolio/TA’s - Collaborate with Senior Programmers/Leads and complete the assigned tasks - Ensures adherence to...

Principal Statistical Programmer - India, Bangalore ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Principal...

We are currently seeking a Statistical Programmer II to join our diverse and dynamic team. As a Statistical Programmer II at ICON, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. Your expertise will contribute to the accurate interpretation of clinical data,...

Senior Biostatistician I - India, Bangalore ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development ICON plc is a world-leading healthcare intelligence...

Overview: - Tasks performed using R. Any Tables, ADaM datasets developed/validated using R: - Data Structures in R (metrices, vectors ), creating datasets using data frame: - Date formatting and character functions in R: - List of packages exposed like DPLYR, TIDYVERSE, HAVEN, ADMIRAL, LUBRIDATE, STRINGRand experienced with functions like Summary, Count,...

At least 5+ years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. - Statistical Programming and SAS hand-on experience - Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data. - Good understanding of ICH and regulatory guidelines - Working knowledge of clinical data...

Job Description:Senior SAS ProgrammerThe Senior SAS programmer leads the programming activities for various purposes including CSRs, DSMBs, interim analyses, manuscripts, etc. Mainly supports statistical programming of statistical analysis plan (SAP)-planned tables, data listings, and graphs for CSRs, as well as integrated summaries of safety and efficacy,...

At least 5 - 6 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. - Accountable for the quality and timely delivery of of enterprise, study and asset level deliverables of standard statistical programming encompassing the following areas: CDISC SDTM, ADaM, and TLF generation - Demonstrate experience working as part of a...

Role & responsibilitiesResponsible and accountable for providing line management leadership to Statistical programming teams working across (ADaM, TLF, SDTM) within ICON Strategic Solutions. Ensure team deliverables are met to the expected quality within agreed timelines. Mentor / develop teams under the guidance of Manager / Sr. Manager or designee. ...

Senior Report ProgrammerICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Clinical Data Science Programmer to join our...