We are seeking a seasoned Clinical Research Associate to support Oncology studies across Ireland and the UK. The ideal candidate will have extensive experience in independent site monitoring, knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, and a life science degree or equivalent industry experience.
The successful candidate will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, administering protocol training, evaluating study site practices, managing study progress, and ensuring proper documentation is maintained.
This role requires flexibility to travel to sites as required. Strong communication and organizational skills, along with attention to detail and ability to work independently, are essential for success in this position.