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  • Experience: 2 to 4 years in the pharma industry, with at least 2 years setting up clinical trial databases (such as Veeva EDC or InForm).Technical Skills:Experience with Python, SQL, R, or SAS.Hands-on experience with Azure Databricks. Roles and Responsibilities:Responsible for design and set-up of study database (EDC and CDMS build) leading upto SDTM datageneration, for data collection in clinical trials, with medium to high complexity.ï‚· Responsible for
    17 september 2026

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