Teams at IQVIA

Support CRAs and RSU by maintaining clinical documents and systems (TMF), handling distribution, filing, archiving, and tracking of study files, CRFs, queries, and clinical supplies. Act as central contact for project communications and may assist on site visits after training.

Assist Clinical Research Associates and Regulatory teams with maintaining trial documents, managing data flow, and coordinating communications. Perform administrative duties related to clinical trials.

The Consultant, Epidemiologist will support epidemiological study design, perform analyses, conduct literature reviews, and collaborate on projects across APAC, ensuring timely delivery of results.