Overview In this role you will provide medical thought leadership to steer strategic decisions, product roadmaps, and market expansion. You will unite Medical Affairs, Medical Safety, and Clinical Affairs to shape...

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 provide medical thought leadership to steer strategic decisions, product roadmaps, and market expansion. You will unite Medical Affairs, Medical Safety, and Clinical Affairs to shape...

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 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 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...