ClinicalProgrammerI

**_Title: Clinical Programmer I_** ** _Hybrid work - Location: Warsaw_** **ABOUT ASTRAZENECA** At AstraZeneca every one of our employees makes a difference to patient lives every day. You may not feel you’re at the frontline of research but your role in changing patients’ lives is critical. Our mission is ambitious, and it takes the skills of a collaborative team to really deliver on what science can do and to always put patients first. Working at AstraZeneca we believe in the potential of our people and our commitment to develop our people beyond what was thought possible. Clinical Programmer I is primarily responsible for providing support to activities related to programming and validation of data cleaning and review listings for ongoing clinical studies with low to medium scope and complexity. This role works under the direction of an experienced programmer. **Responsibilities include:** **Core Competencies:** • Responsibilities include (but not limited to) design, development, implementation and validation of programs created in SAS/Python/R or dashboard applications, to process, analyze and report clinical trial data for review by clinical study teams. • Works within established frameworks and ensure high quality built into own deliverables. • Under guidance, creates catalogue of reports to aid data cleaning activities with low to medium complex in scope, but not limited to: o Automate manual checks. o Automate reconciliation and program edit checks for TPV data to ensure quality. o Create tools and repository to minimize data errors at source for collection of lab reference ranges. o Program reports to identify missing pages and detect errors at Subject level. o Create reports to measure metrics that can help assess data cleaning status. o Create visualizations and dashboards to identify discrepancies and trends in EDC and TPV data • Maintain created catalogue of reports and perform any required updates (PPC) based on ongoing changes to requirements. • Provid