We are looking for an experienced Clinical Research Associate, willing to work within the field of oncology. The Senior Clinical Research Associate will Perform site qualification, site initiation, and closeout visits, ensuring regulatory and protocol compliance. Visits may be on-site or remote.

Monitor clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol. Coordinate activities to set up and monitor a study. Senior CRAs manage trials and support Project Managers, training junior staff and interacting with clients.

In this CRA role, you’ll utilise your therapeutic knowledge in Oncology to oversee clinical studies. Working at the core of clinical research, you’ll be exposed to protocols and experience a dedicated partnership with your team. As a CRA you are the main sponsor representative, providing key project updates.

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.