Top Tech Jobs & Startup Jobs in Pune

As a Senior Statistical Programmer, you will leverage SAS programming skills and CDISC standards to support clinical trials, perform data manipulation, and generate reports.

The Principal Statistical Programmer will independently manage statistical programming for clinical trials, overseeing CRO deliverables, generating datasets, and ensuring compliance with FDA regulations.

The Principal Statistical Programmer will generate datasets and reports, oversee CRO's programming deliverables, and ensure compliance with FDA regulations, while collaborating with various teams in clinical trials.

This role involves managing project operations, supporting leaders with scope reconciliations and invoicing, ensuring documentation compliance, and facilitating team collaboration.

The Principal Statistical Programmer develops and validates SAS and R programs, oversees CRO deliverables, and ensures high-quality statistical reporting for clinical trials.

The Clinical Data Engineer serves as an expert in USDM, driving digital protocol generation and enabling seamless data flow across the clinical development lifecycle, while collaborating across functions to optimize processes and ensure compliance with industry standards.

The Senior Clinical Data Manager oversees data management tasks from study initiation to database lock, ensuring high-quality data delivery, adherence to timelines and budgets, and leading project activities with minimal supervision. Responsibilities include user acceptance testing, data cleaning, project documentation, training staff, and managing client communication.

The Senior Statistical Programmer will support and lead clinical trials by performing data manipulation, analysis, and reporting using SAS programming. Responsibilities include generating SDTM and ADaM datasets, validating programming, creating reports, and collaborating with cross-functional teams.

The Principal Statistical Programmer provides technical leadership in SAS and R programming for clinical trial data analysis, reporting, and regulatory submissions, ensuring compliance and quality control while managing teams and resources.

The Principal Statistical Programmer leads SAS and R programming for clinical trials, ensuring compliance, quality, and effective communication with stakeholders.