1 - 6 years
20 - 25 Lacs
Posted:1 day ago|
Platform:
Work from Office
Full Time
What Youll Do
Lead programming activities across studies and clinical development phasesOversee CRO deliverables for quality, timeliness, and regulatory complianceProvide technical oversight for SDTM, ADaM, Define.xml, DRGs, and TLFs
Were Looking For8-12 years clinical programming exp. with leadership exposureExpert SAS skills (Base, Macro, SQL); strong SDTM, ADaM, Define.xml, TLF experienceBachelor's/Master's in Statistics, CS, Life Sciences, or related fieldProven CRO management experience across selection, oversight, and deliveryStrong Hands-on R skills for exploratory analysis and visualizationPreferred: Familiarity with Pinnacle 21, CDISC validation, ISS/ISE, and automation tools
AVE-Promagne Business Solutions
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