Jobs 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.

Lead the Data, Technology, and Advisory Services growth in JAPAC, driving strategy, client engagement, and team development across multiple sectors.

Lead design of strategic, operationally feasible solutions for large, multi-region clinical studies. Drive feasibility, site selection, patient recruitment, budgeting, proposal development, client engagement, and handover to delivery teams while supporting revenue growth and cross-functional collaboration.

Prepare and review regulatory submissions to support clinical trials and marketing authorisations. Lead/regulate complex projects, perform technical writing, manage budgets, mentor junior staff, present to clients, propose or revise SOPs, and support regulatory initiatives under Regulatory management.

The Associate Account Director develops new business clients in the pharma sector, manages client accounts, collaborates on sales strategies, and ensures client satisfaction through effective service delivery.

The Clinical Operations Manager oversees clinical study deliverables, conducts interviews for hiring, manages staff resources, ensures compliance with regulations, and participates in quality improvement initiatives.

The role involves building and adapting health economic models, conducting analyses, collaborating with stakeholders, and preparing reports and presentations.

As a Senior CRA, you will conduct site visits, monitor trial progress, manage documentation, communicate with stakeholders, and ensure compliance with clinical research regulations.

Analyze and support epidemiological studies, perform data analyses, communicate findings, and collaborate with project teams in real world evidence generation.