Jobs at IQVIA

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 Data Analyst role involves collecting and analyzing pharmaceutical sales data, delivering reports, investigating anomalies, and suggesting process improvements. Requires collaboration with stakeholders to ensure data integrity and decision-making support.

The Clinical Research Coordinator supports the execution of clinical trials through administrative tasks, patient enrollment, data management, and communication with study monitors.

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

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

The Senior Contract Associate oversees preparation, negotiation, and finalisation of clinical trial agreements. Responsibilities include contract efficiency, collaboration with stakeholders, and maintaining compliance with regulations.

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