Found Description
IQVIA in Madrid is seeking a Lead Programmer with over 8 years of experience in statistical programming within the pharmaceutical or CRO environment. The role involves leading the development and validation of CDISC-compliant datasets while collaborating with various teams to support early-phase decision-making.
The ideal candidate will have expert-level proficiency in SAS programming and a solid understanding of early-phase clinical trial designs. Strong communication and stakeholder management skills are essential.
This position offers opportunities for mentorship and contributions to regulatory submissions.
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