https://talentsoft.akka-technologies.com/handlers/offerRss.ashx?LCID=2057&Rss_JobCountry=96 en-GB https://talentsoft.akka-technologies.com/Pages/Offre/detailoffre.aspx?idOffre=30636&idOrigine=502&LCID=2057&offerReference=2024-30636 OPERATIONS/CONSULTING Permanent contract Bangalore <b>Category : </b>OPERATIONS/CONSULTING<br /> <b>Contract : </b>Permanent contract<br /> <b>Position description : </b><br /> An experienced statistical programmer with a strong background in the Life Sciences industry. Skilled in data analysis , statistical modeling , and programming , with a proven track record of contributing to the successful execution of clinical trials and research projects. Committed to maintaining the highest standards of data quality , regulatory compliance , and efficiency in statistical programming. Provides statistical programming expertise to deliver high quality Develop Analysis Data Model (ADaM) datasets Develop (Tables, Figures and Listings (TFL) Output and Programming Specification [ OPS ] from the Statistical Analysis Plan [ SAP ] or a related document Program and validate standard ADaM utility Statistical Analysis Software [ SAS ] macros or R function/package following good programming practices  Statistical Programming: Proficient in SAS, R, and other statistical software.  Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting.  Data Management: Data validation, cleaning, and integration.  Regulatory Compliance: Knowledge of FDA and EMA guidelines. Programming Languages: SAS, R, Python.  Statistical Analysis: Data modeling, hypothesis testing, and statistical inference.  Data Visualization: Generating graphs, charts, and visual representations of data.  Team Collaboration: Effective communication and teamwork in cross functional environments.  Problem Solving: Analyzing complex data challenges and finding innovative solutions.<br /><br /> Statistical Programming: Proficient in SAS, R, and other statistical software.  Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting.  Data Management: Data validation, cleaning, and integration.  Regulatory Compliance: Knowledge of FDA and EMA guidelines. Programming Languages: SAS, R, Python.  Statistical Analysis: Data modeling, hypothesis testing, and statistical inference.  Data Visualization: Generating graphs, charts, and visual representations of data.  Team Collaboration: Effective communication and teamwork in cross functional environments.  Problem Solving: Analyzing complex data challenges and finding innovative solutions.<br /> <b>Location : </b>Bangalore<br /> <b>Language / Level : </b><br /> English : 4 : Native / Bilingual level<br /> Tue, 13 Feb 2024 12:42:51 Z