We're a general, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Clinical Research

Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.



Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.

Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits. Conduct source document verification for compliance, patient safety, and veracity of data. Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.

Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate. Excellent interpersonal, oral, and written communication skills in English Ability to work with little or no supervision Proficiency in Microsoft Office, CTMS and EDC Systems 5+ years of experience as a Clinical Research Associate 4-year university degree or RN/BSN in Nursing

📌 [Oncology]Clinical Research Associate (Barcelona)
🏢 Worldwide Clinical Trials
📍 Barcelona