Overview In this role you will contribute to Phase I–IV clinical trials within IQVIA Biotech’s EU Clinical Monitoring team. You will oversee site performance, ensure adherence to GCP/ICH, and coordinate monitoring...

Overview As Senior Manager, Clinical Trial Planning, you will support Clinical Trial Teams to manage trial timelines and enable planning systems. You will own MSP templates, drive Planisware adoption, and develop...

Overview As a Clinical Research Associate II in IQVIA’s sponsor-dedicated model, you oversee site monitoring and ensure adherence to GCP/ICH. You collaborate with sites to drive recruitment, training, and data...

Overview In this role you drive the planning, execution, and oversight of global clinical trials to meet timelines, quality, and regulatory expectations. You collaborate with CROs, internal teams, and investigators to...

Overview In this role you will support a single sponsor as a Clinical Research Associate within IQVIA’s FSP model. You’ll manage and monitor sites across the country, contribute to patient recruitment plans, and...

Overview In this Senior CRA role, you will lead on-site monitoring within our sponsor-dedicated model in the Netherlands, ensuring GCP/ICH compliance and high-quality site performance. You will partner with sites and...

Overview As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial...

Overview In this role you will work as a dedicated CRA within IQVIA’s sponsor-aligned clinical FSP setup. You’ll manage sites and monitor study progress across the country, focusing on patient recruitment and protocol...

Overview In this role you lead the Allucent Data Management team to ensure high-quality, regulatory-compliant clinical data from setup to lock. You will collaborate with cross-functional groups and external partners...

Overview In this role you lead trial monitoring staff in-country, ensuring high-quality clinical operations and adherence to ICH/GCP. You work with regional leaders to meet timelines and quality standards, while...