Clinical Programming Lead

5 days ago

anand, India beBeeStatistical Full time

We are seeking a highly skilled Senior Statistical Programmer to support the entire clinical programming process across various studies.The ideal candidate will possess exceptional technical expertise, be self-sufficient, and able to effectively collaborate with cross-functional and global teams.Key ResponsibilitiesProgram, validate, and maintain clinical trial datasets and outputs using SAS and R programming languages.Lead and execute the full spectrum of statistical programming deliverables, including data analysis and visualization.Requirements:Prior experience working in global or geographically distributed teams is essential.In-depth knowledge of CDISC standards and regulatory submission requirements is necessary.Experience supporting FDA and PMDA submissions is highly desirable.Clinical Programming ExpertiseOur team requires a Senior Statistical Programmer who can efficiently program, validate, and maintain clinical trial datasets and outputs using SAS and R. The successful candidate will have a strong understanding of clinical trial data management and regulatory requirements.Clinical Trial Data ManagementDevelop, implement, and maintain clinical trial databases and data sets.Ensure data quality, integrity, and compliance with regulatory requirements.Collaborate with cross-functional teams to design and implement data collection systems.Statistical Programming DeliverablesThe Senior Statistical Programmer will lead and execute the full spectrum of statistical programming deliverables, including data analysis and visualization. The ideal candidate will have excellent analytical skills, attention to detail, and effective communication skills.Data Analysis and VisualizationAnalyze complex clinical trial data using statistical software such as SAS and R.Create high-quality visualizations and reports to present findings to stakeholders.Collaborate with data scientists to develop predictive models and identify trends.

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