Manage all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files, ensuring data quality, compliance with SOPs, regulatory requirements, and study completion on time and within budget.

Perform all aspects of CRA duties from site selection, site initiation, routine monitoring visits (on-site and remote), and close-out visits through to database lock. Be fully embedded in the client's study team and have a dedicated ICON functional manager to support you. Oversee all aspects of study site management to ensure high-quality data.

You'll handle site management (including start-up), both on-site and remotely, on 2-3 trials, working on projects from our client base of small to big pharmaceutical, biotechnology, medical device and consumer health companies. Previous experience monitoring oncology and/or respiratory clinical trials is required.