Overview As Senior Director Non-Clinical Development, you shape and execute the non-clinical strategy across Pharming’s biopharmaceutical products, aligning with clinical and CMC plans. You lead a small scientific...

Overview In this role you drive the end-to-end execution of global clinical trials, partnering with cross-functional teams to ensure on-time delivery within regulatory and quality standards. You lead with autonomy,...

Overview In this role you will monitor clinical studies at investigative sites to ensure trial activities align with protocol, SOPs, and ICH-GCP. Based in Belgium or the Netherlands with remote work and regular site...

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 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 As a Sr. Project Manager at Allucent, you coordinate and drive clinical trials from start-up through delivery, predominantly in Oncology, Neuroscience, Immunology and Infectious Diseases. You lead...

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...