Clinical Trials Monitor

We are looking for a Clinical Trials Monitor to join team, to be responsible for clinical trial monitoring activities of the investigator sites for the FLIP2 Trial and the MET-FINGER Trial.

The FLIP2 Trial is a placebo-controlled double blinded randomised trial to assess the safety and efficacy of a live biotherapeutic compared to placebo, in reducing the risk of preterm labour in a cohort of women predefined as at high risk. ~360 participants will be recruited across up to 8 sites in the UK and EU. The trial aims to determine whether administration of a live biotherapeutic in the second trimester of pregnancy in women at high risk of preterm birth leads to a reduced incidence of preterm birth

The MET-FINGER Trial is a randomised, controlled, parallel-group, multicentre trial testing the FINGER 2.0 multimodal lifestyle-based intervention with a pharmacological trial-within-trial including metformin treatment. The trial aims to look at the impact of this intervention on change in cognition in a population of older adults at increased risk of dementia. A total of 600 participants will be recruited across 3 sites in the UK, Finland, and Sweden.

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.

This role requires visits to national and international investigator sites, and as such will involve travel with occasional overnight stays.

You must have a science degree (BSc), or equivalent vocational qualification, or equivalent experience.Proven clinical trial monitoring experience and knowledge of the current relevant regulations is vital.
The opportunity to continue your career at a world-leading institution and be part of our mission to continue science for humanity Benefit from sector-leading salary and remuneration package (including 39 days off a year and generous pension schemes) Get access to a range of workplace benefits including a flexible working policy from day 1, generous family leave packages, on-site leisure facilities and a cycle-to-work schemeInterest-free season ticket loan schemes for travel Be part of a diverse, inclusive, and collaborative work culture with various and resources designed to support your personal and professional .