Teams at IQVIA

Perform site selection, initiation, monitoring, and close-out per protocol, contract, SOP and GCP. Oversee multiple studies/sites, train and communicate with sites, evaluate compliance and quality, report issues to PM/manager, track enrollment/CRF completion/data queries, maintain monitoring documentation and visit reports, manage site study finances, collaborate cross-functionally, and complete other manager-assigned tasks.

Lead and manage site activation activities across a multi-country region, overseeing site selection, regulatory/ethics submissions, contracting, and start-up execution. Develop and implement site activation plans, provide regulatory intelligence, coordinate stakeholders, maintain tracking systems and reporting, support bids, and ensure compliance with ICH-GCP, protocol, and company standards.

Lead development of analytic datasets and longitudinal analyses for oncology observational studies using claims, EHR, and lab data. Build cohorts, define/validate variables, perform QC, conduct survival and regression analyses, develop TFLs, and contribute to protocols and reports. Provide technical, programming, and statistical expertise while managing multiple complex studies and communicating results to stakeholders.