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...

The Role CSL is looking for a Principal Programmer to take technical ownership of statistical programming across a compound or programme, not just a single study. You'll be the person who sets how the programming gets...

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 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...

CSL in Maidenhead is seeking a Principal Programmer to take technical ownership of statistical programming across a programme of trials. You'll set how the programming is done across multiple studies, lead both...

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 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...

Principal Clinical Scientist (Senior Clinical Scientist level also considered) The Role We're looking for a clinical scientist — someone who has been the scientific lead for clinical studies before, from protocol...

As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs,...