Teams at IQVIA

The CRA I supports clinical research by monitoring sites, ensuring compliance with regulations, and maintaining communication with investigative sites. Responsibilities include site visits, protocol training, and documentation preparation.

Lead end-to-end development, validation, and operationalization of connected medical device and digital health solutions for respiratory trials. Partner with strategy to evaluate solutions, own startup execution from approval through Business Go‑Live, coordinate cross-functional teams (Engineering, QA, Regulatory, Data, Operations, vendors), ensure readiness, quality, and compliance, manage risks/escalations, and support commercialization and stakeholder communications for scalable study deployment.

Perform data analysis using Excel and SQL, build reports and PowerBI dashboards, deliver client presentations, support ad-hoc and scheduled analytics requests, and collaborate with account teams to provide actionable insights for healthcare clients.