Jobs at IQVIA

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.

Serve as a client-facing SaaS implementation and support expert for a clinical eSource platform. Lead client onboarding, deliver training, troubleshoot technical issues, manage support tickets within SLAs, gather configuration requirements, and collaborate with Engineering, Product, Sales, and Project teams. Support audits, demos, validation and contribute to documentation and testing while traveling to client sites as needed.

Lead end-to-end site start-up and activation activities across multiple sponsors and therapeutic areas. Coordinate site feasibility, ethics and ICF submissions, contract and budget negotiations, and maintain site/study records. Serve as primary contact for investigative sites, communicate timelines and risks to internal stakeholders, and provide operational guidance to junior team members to ensure timely, compliant site activation and ongoing site maintenance.

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.

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.

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.

Support clinical research sites on PAH and IPF studies to improve patient recruitment, retention and trial delivery through education, site engagement, training, data-driven strategies, referrals, reporting and site visits.

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

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