Teams at IQVIA

Develop, validate, and review SDTM domains; perform CRF annotation; ensure CDISC compliance and regulatory submission readiness (define.xml, P21, SDRG); use advanced SAS programming; SQL/Python knowledge advantageous.

Lead delivery of clinical studies or study components, managing cross-functional teams to meet contract, quality, timeline and financial goals. Oversee planning, risk management, vendor relationships, change control, stakeholder communication, and staff development while ensuring compliance with ICH GCP and corporate processes.

Deliver and support client projects in the life sciences sector by analyzing requirements, developing proposals and documentation, performing quantitative/qualitative analyses, creating presentations and client deliverables, and occasionally leading small teams while learning consulting methodologies.