Teams at IQVIA

Lead planning, execution, and delivery of regional or global clinical trials to meet timelines, budgets and regulatory standards (ICH-GCP). Manage project performance, risks, vendors, and finances; mentor junior staff and represent IQVIA to clients.

Support Project Leader in clinical trial delivery by coordinating schedules, cost control, risk management, change control, finance activities, dashboards, study file oversight, meeting coordination, vendor management, and audit support while ensuring timely system updates and resource management.

The Site Activation Specialist (SAS) manages site start-up activities, including ethics submissions, budget negotiations, and communication with internal and external stakeholders to ensure compliant site activation.