CRA II

As an experienced Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Within this client dedicated program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true "one team" approach that provides limitless opportunity to develop through training, mentorship, and support from leadership. Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock incl. on-site, remote and risk-based monitoring. You will be embedded in our client's study team and have a dedicated ICON line manager to support you, overseeing all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports.