This contract position ensures data collected for clinical studies is accurate and traceable, assists in site management, and develops clinical study materials. You will support site identification, conduct monitoring visits, perform source data verification, and track regulatory document submissions.
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Be a contributor to routine, consolidated Study Monitoring updates by performing all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock. You will be embedded in our client's study team and have a dedicated ICON line manager to support you, while overseeing all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports.
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, while ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct.
Join our team in Italy as an experienced CRA II or Senior CRA, where you'll monitor oncology clinical studies. This remote position offers reasonable travel and work/life balance. You'll ensure studies are conducted per protocol, SOPs, and regulations, and contribute to study setup, investigator identification, and regulatory submissions. Your voice will be heard in this smaller CRO.
Join our dynamic team as a Clinical Research Associate at ICON, and play a pivotal role in advancing innovative treatments. Responsibilities include conducting site visits, ensuring protocol compliance, performing data review, and contributing to study documentation.
As a Clinical Research Associate II, you will monitor clinical studies at investigative sites, ensuring they're conducted and reported per protocol. You'll coordinate activities, identify investigators, and help prepare regulatory submissions with an impeccable eye for detail. You will identify risks and take responsibility for the quality of your work.
Provides overall support to study sites and clinical project teams engaged in clinical research studies, adhering to applicable protocols, SOPs, and regulatory requirements. Acts as point of contact for study sites and expected to work independently in providing support to CRA and sites. Can have increased focus on training and development of junior staff members and can act as Lead In-house CRA.
Monitor and own the progress of clinical studies at investigative sites, ensuring clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).