We’re a global, 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 integral 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.
Join Worldwide Clinical Trials for an unparalleled CRO experienced, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial.
Our commitment to advancing clinical research is cultivated in a supportive, team‑oriented atmosphere,



with our hands‑on leadership and dedicated team members working together to innovate and solve complex challenges for our customers.
Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow‑up for all safety events by site personnel
IRB approval, informed consent, lab certification etc.)
Ability to contribute to a team remotely
Proficiency in Microsoft Office, CTMS, and EDC Systems
Four‑year college curriculum with a major concentration in life science preferred but not required, OR
Two‑year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) Proficiency in English and at least one of the following languages: German, Polish or Italian.

📌 In-House Clinical Research Associate (La Coruña)
🏢 Worldwide Clinical Trials
📍 La Coruña