PRA Health Sciences

You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas and assist other CRAs with co-monitoring activities both remote and on-site. As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.

As an experienced Clinical Research Associate, you will be joining a fast-paced, dynamic study design where you will be embedded within a global pharmaceutical client. 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, overseeing all aspects of study site management to ensure high quality data.