Clinical Trial Assistant

Working as a partnership, both Isle of Wight NHS Trust and Portsmouth Hospitals University NHS Trust have a shared vision for excellence in care for our patients and communities; with a set of strategic aims underpinning how we will achieve this.

The single corporate service is delivered across both organisations. You may be based at either IWT or PHU and individuals may be required to undertake business travel between sites. For leaders managing staff across multi-site locations, you will need to be visible and provide in person leadership. The arrangements and frequency will be agreed locally.

This post is only open for applications for internal applicants for Portsmouth Hospitals University NHS Trust and Isle of Wight NHS Trust

NHS Band 3 Salary: £25,760 - £27,476 per annum

Hours Per Week: Full time 37.5 hrs

Contract Type: Permanent

Are you looking for a new & different role, do you want to make a difference and improve health outcomes? Do you want to be at the forefront of new treatments & technology? If yes, this role maybe for you, as it combines clinical patient and participant contact with effective administration skills. The role of a clinical trials assistant is key in supporting a multidisciplinary team to set up and deliver clinical research studies.

We have a B3 position for an enthusiastic, motivated, and highly organised individual to join our team. This is a full-time position worked over a Monday to Friday flexible working pattern. Occasional weekends and public holidays may be required with notice. The role is based at the David Hide Asthma & Allergy Research Centre, IOW site. The Centre is a registered charity based in a purpose-built building at St Mary’s Hospital IOW NHS Trust on the Isle of Wight and its activities are overseen by a Board of Trustees. The David Hide Asthma & Allergy Research Centre has become internationally renowned for the excellence of its research with an active research programme focusing on various aspects of childhood and adult asthma and other allergic diseases as well as the prevention of allergy. For more information about the Centre please follow the link: http://www.allergyresearch.org.uk/

For full job details and person specification please refer to the Job Description

Interviews will be held on the 9th December 2026.

Responsibilities

You will be responsible for supporting the day to day running of clinical trials from the National Institute of Health Research (NIHR) Portfolio and external grant funded research projects. You will work across a range of studies, which may include interventional & observational research.; You will be working with an experienced supportive team who are passionate about offering research opportunities to participants and patients to improve health outcomes.; The role is varied as each study and subsequent clinic requirements can be different, this brings the opportunity to develop wider skills such as basic lab sample processing, handling, and shipping of samples.; As a member of our team, we are committed to your personal and career growth and actively encourage continuous development. This is provided through access to organisational study days, research specific training and identified learning at appraisal. We can offer development opportunities to experience clinical research in other areas at the Queen Alexandra site or across the region with other partner organisations.; Working as part of a team this role supports the smooth running of clinical research clinics and studies. The administrative functions of the role include creating and preparing localised study templates and participant packs, capturing and transcribing data into a variety of different data management platforms and responding to data queries. You will be ordering, tracking and managing receipt and supplies of clinical trial materials and general supplies for the clinics.; The clinical facing elements of the role are to support the research team with the running of face-to-face research clinic visits. You will plan and prepare for the clinics, arrange appointments, and follow up visits. Clinical tasks may include phlebotomy, basic vital signs, allergy skin prick testing, lung function tests, pregnancy testing, height/weight measurements under the supervision of registered professionals. Full training will be provided.

Requirements

NVQ 3 level of knowledge and training.; Computer literate, with knowledge of patient administration & Microsoft office systems.; Completed Care Certificate or ability to complete within 3 months of appointment.; Good organisational skills.; Excellent communication skills, both written and spoken.; Ability to work as part of a team, but also able to use own initiative and work without supervision.; Innovative and adaptable to change.

Nice to have

Good Clinical Practice (GCP) training for research.; Previous experience of clinical trials or research projects.; Experienced in phlebotomy and vital signs observations.; An understanding of medical terminology and clinical processes.