SeniorPrincipalStatisticalProgrammer

**Job Description Summary** Job Description Summary Responsible for all statistical programming/data review reporting and analytics development aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high-quality deliverables. Complies with project / study standards and specifications following internal and regulatory guidelines. Oversees programming style, quality of statistical reporting & compliance with timelines. **Job Description** **Key Responsibilities** * Lead statistical programming activities for several studies or drive the implementation of data analytics reports. Make decisions and propose strategies at study or project level. * May act as functional manager for local associates including providing supervision and advice on functional expertise and processes. * Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical aspects (timelines, scope, resource plan), e.g. as representative in study or project-level team. * Ensure project-level standardization. Provide and implement programming solutions; ensure knowledge sharing. * Act as expert in problem-solving aspects. * Ensure timely and quality development and validation of datasets and outputs for regulatory submissions/interactions, safety reports, publications, post-marketing activities etc .Leads/co‐leads novel projects within the team -Generates innovative ideas within own team and /or project team /functional community **Essential Requirement** * Demonstrates strong proficiency in **SAS** for the analysis and summarization of clinical trial data. * Has served as a **Trial Programmer** or in a comparable programming role with end‑to‑end study responsibility. * Possesses experience in the **development and/or review of critical study documents** , includ