Seeking a Clinical Data Standards/Clinical Programmer with robust knowledge of CDISC standards (CDASH, SDTM, ADaM, ARDS), positive understanding of the clinical trial lifecycle, and intermediate SQL skills. The role involves clinical data programming, standards implementation, dataset validation, metadata management, and supporting regulatory submissions. Candidates should have experience collaborating with cross-functional teams and working in customer-facing environments within pharma, biotech, or CRO industries.
Robust analytical, communication, and problem-solving skills are required.
📌 Clinical Trial System Noida
🏢 NR Consulting
📍 Noida
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