Salary: £40,809- £49,818 per annum plus benefits
Location: Stadium House, White City Campus (currently hybrid working)
Job Summary
We are looking for a Clinical Trial 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 CARE Trial and the BACHb Trial.
The CARE Trial is a 52-week multi-centre, open label, 2-arm randomised controlled trial (CTIMP) taking place at 25 sites in the UK, recruiting 1,352 participants. The trial aims to determine the clinical effectiveness, safety and cost-effectiveness of ICS-formoterol reliever therapy compared with SABA reliever therapy in children with asthma aged 4 to 11 years.
The BACHb trial is a multicentre open-label randomised clinical trial of respiratory support in infants with acute bronchiolitis taking place at 50 sites in the UK, recruiting 1508 infants. The aim of the BACHb trial is to evaluate the clinical and cost-effectiveness of the use of high-flow nasal cannula (HFNC), in comparison to other forms of respiratory support, separately in two distinct populations of infants with bronchiolitis: moderate and severe.
Duties and responsibilities
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 investigator sites, and as such will involve travel with occasional overnight stays. There may also be a requirement for other international travel for training and monitoring purposes.
Essential requirements
- 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.
Further Information
This post is full-time and fixed term for 12 months in the first instance. The exact work pattern can be flexible and will be discussed at the interview.
You will be based at Stadium House, White City campus, close to Wood Lane and White City tube stations.
We offer excellent benefits, such as a generous pension scheme, cycle to work scheme, generous holiday allowance, flexible working and access to comprehensive in-house training and development programmes.
Should you have any queries please contact Christina Prechtl – [email protected] and Mary Cross – [email protected].
For technical issues when applying online, please contact: [email protected]
The College is currently trialling a Work Location Framework until early 2023. Hybrid working may be considered for this role and the role holder may be expected to work 60% or more of their time onsite, with 40% the minimum time spent onsite. The opportunity for hybrid working will be discussed at interview.
Closing date: 12/07/2023