Global Veterinary Careers is assisting a Petersfield-based, RCVS-accredited practice to recruit a Small Animal Veterinary Surgeon. This GP role offers a 4‑day week, no night shifts, and a salary up to £60,000...

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 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 deze field-based rol ben je de klinische expert voor een portfolio medische producten en dien je als trusted partner voor zorgprofessionals. Je draagt bij aan commerciële groei door klinische knowhow te...

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 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...