Jobs at IQVIA

Support site activation activities for clinical studies: prepare, review, distribute and track regulatory and contractual documents; maintain databases and project trackers; coordinate with Site Activation Manager and project teams to ensure timely site start-up.

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

The Account Director manages key client accounts, ensuring satisfaction and growth while collaborating on strategic plans and overseeing project execution.

The Consultant will manage end-to-end market research projects, apply qualitative and quantitative methodologies, and deliver actionable insights to clients in healthcare.

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.

The role involves site monitoring, managing study progress, ensuring regulatory compliance, and communicating effectively with sites and project teams.

The Senior Clinical Research Associate will perform site monitoring and management tasks to ensure compliance with study protocols and regulatory guidelines, manage recruitment plans, and collaborate with study team members for project execution.

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.

The Clinical Trial Assistant supports clinical projects by managing documentation, communicating with teams, and ensuring compliance with regulations.

The Site Activation Specialist will manage site activation, documentation, and coordination between departments while tracking site performance and maintaining contact with investigative sites.