Lead PK/PD Statistical Programmer - Early-Phase & TLFs

IQVIA is seeking a Lead Programmer in Barcelona, Spain to develop and validate CDISC-compliant datasets and lead programming for Phase I trials. This role involves collaborating with Clinical Pharmacology and contributing to regulatory submissions.

The ideal candidate will have over 8 years of experience in statistical programming within a pharmaceutical environment and demonstrate expertise in SAS and CDISC standards. Strong communication and stakeholder management skills are essential.