At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic leadership for complex global clinical trials, partnering directly with...

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...

Clinical Monitoring Analyst (Cluepoints) - Remote London, United Kingdom Budapest, Hungary Reading, Berkshire, United Kingdom Bloemfontein, South Africa Dublin, Ireland Centurion, South Africa Barcelona, Spain Sofia,...

SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100...

Title: Clinical Application Specialist, PMLS, NWEU Clinical Application Specialist – Northwest EU Location: Netherlands | Sweden Affiliates to a Mindray office in the Netherlands which is office-based or a Mindray...

Role & Responsibilities The IQVIA Patient Centered Solutions group has an opportunity for a Manager to join the team to support Licensing & Distribution activities. In this role you will be responsible for managing...

Описание: At IQVIA, Patient & Site Centric Solutions (PSCS) brings together capabilities focused on improving the experience and outcomes of patients, sites and customers across clinical development. We are looking...

Johnson & Johnson is looking for a driven Senior Clinical Research Manager to join our Clinical Operations team in The Netherlands. This role involves managing a team responsible for trial execution in oncology while...

Overview In this role you will establish and govern SDTM standards to ensure data quality and consistency across trials. You will oversee sponsor activities with Biometrics vendors and align data collection with...

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...