Requisition Number
6073

Employment Type*:
Regular

Who we are

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 general team of almost 2,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

What you will do
- 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
- Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.)




- Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
- Perform feasibility studies/site identification activities for potential sites, as requested

What you will bring to the role
- Excellent interpersonal, oral, and written communication skills in English and local language
- Ability to contribute to a team remotely
- Strong customer focus, ability to interact professionally with a sponsor contact
- Proficiency in Microsoft Office, CTMS, and EDC Systems

Your background
- 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.) or other experience deemed relevant

Why Worldwide
At Worldwide, we balance fun with the serious business of changing lives. We have a values

📌 In-house Clinical Research Associate (Madrid)
🏢 Worldwide Clinical Trials
📍 Madrid