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ABOUT THE ROLE

We are looking for a Clinical Trials Monitor to join the UKCRC registered Imperial Clinical Trials Unit (ICTU) team, to be responsible for clinical trial monitoring activities of the investigator sites for the WARRIORS Trial.
The WARRIORS Trial is an international, randomised controlled trial investigating whether early endovascular aneurysm repair (EVAR) reduces the risk of aneurysm-related mortality and rupture in women with small abdominal aortic aneurysms (AAA) compared to current standard of care. The trial aims to enrol 1,112 participants across approximately 100 sites globally, spanning 12–18 countries. In the UK specifically, 15–18 centres will recruit a total of 150 participants. A 250-participant Vanguard phase will first assess the feasibility of recruitment and the safety of early EVAR before the full trial rollout. The primary composite outcome—aneurysm-related mortality and rupture—will be assessed five years after randomisation.

WHAT YOU WOULD BE DOING

This varied role includes monitoring, feasibility, initiation, enrolment, follow-up, and close-out of investigator sites as well as archiving, with guidance from the Clinical Trial Managers and Operations Managers. You will oversee the progress and performance of the investigator sites, including efficient recruitment and reliable data collection, and ensure project objectives and timelines are met. You will ensure that the clinical trial is being conducted in accordance with contractual agreements, trial protocol, trial-specific processes and systems, SOPs, regulatory and ethical requirements and ICH-GCP guidelines.
In addition to traditional monitoring responsibilities, the post-holder will contribute to embedded qualitative research activities within the trial. You will receive training in relevant qualitative methods and support the collection and documentation of qualitative data during site interactions. These insights will play an important role in improving recruitment strategies, site communication, and trial delivery across all participating centres.
This role requires visits to national and international investigator sites, and as such will involve travel with occasional overnight stays.