(Summary generated by AI based on the full job description)
The project involves building a unified ecosystem for Risk-Based Quality Management (RBQM) in the pharmaceutical domain. Key technologies include R and working with CDISC SDTM clinical trial data, plus QTL and statistical monitoring. Responsibilities include developing and maintaining R analytical solutions, creating and automating QTL reports, configuring study-specific QTL logic, performing data validation and quality checks, documenting analytical logic and collaborating with cross-functional stakeholders.

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