Teams at IQVIA

The Senior Clinical Research Associate will monitor and manage clinical trial sites to ensure compliance with protocols, regulations, and sponsor requirements, while collaborating with teams to enhance study execution.

This role involves monitoring clinical centers, ensuring compliance with study protocols, and maintaining communication with investigators. Responsibilities include site visits, participant recruitment oversight, and quality control of studies.

The Senior Clinical Research Associate will oversee clinical trial sites, ensure compliance with regulations, and manage study progress, coordinating with investigators and project teams.