Clinical research associate
Pubblicato il 31-08-2026 - Worldwide Clinical Trials in Italia
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, a global team of over 3,500 experts. Our mission is to work with passion and purpose everyday to improve lives and we are looking for others who value this same pursuit.
Why Worldwide We believe everyone plays an important role in making a difference for patients and their caregivers. From our hands‐on, accessible leaders to cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. What Clinical Operations Does At Worldwide At Worldwide Clinical Trials,
we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
What You Will Do
Responsible for site qualification, initiation, interim monitoring, site management, and study close‐out visits. Provide mentoring and guidance to less experienced CRAs and site staff when needed. Document site visit findings via written reports. Assess, monitor, and train study site staff on protocol adherence as required. Review study subject safety information and informed consent. 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. Provide applicable updates for site related documentation for filing in the Trial Master File (TMF). Ensure site compliance with IP receipt, accou