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IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to lead programming efforts for centralized monitoring across multiple study sites. This remote role supports the CM strategy, develops QTL/KRI/data quality assessments, and ensures CMP alignment with study protocols. The ideal candidate has at least 3 years in pharmaceutical R&D with SAS experience, strong data management skills, and excellent communication in English. No UK visa sponsorship for this role is available. J-18808-Ljbffr
