About the role
Job Description
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/
Key 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.
For full job details and person specification please refer to the Job Description
Qualifications
Essential :
* 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.
Desirable :
* Good Clinical Practice (GCP) training for research. * Previous experience of clinical trials or research projects.
Skills and Knowledge
Essential :
* 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.
Desirable :
* Experienced in phlebotomy and vital signs observations. * Previous experience of clinical trials or research projects. * An understanding of medical terminology and clinical processes.
Additional Information
The health and wellbeing of our staff is at the forefront of everything we do. We are proud to be able to offer our staff some fantastic benefits including our on-site Nursery, access to our free Beach Hut for those long summer days, our on-site Wellness Centre including a gym and a swimming pool, access to our fantastic staff networks including LGBTQ, Race Equality and DisAbility, and awards ceremonies to recognise your achievements. We believe we can offer support to all of our staff when they need it the most.
We welcome the unique contributions that you can bring in terms of your education, opinions, culture, ethnicity, race, sex, gender identity and expression, nation of origin, age, languages spoken, veteran’s status, colour, religion, disability, sexual orientation, and beliefs.
For more information, please see our People and OD Strategy 2026
Smoke Free Policy:
All of our hospitals operate a strict no smoking policy. Smoking cigarettes or tobacco products is not allowed on any of the grounds or in any of the buildings run by us. This applies to patients, staff, carers and visitors to Trust premises.
Our goal is to improve the health and wellbeing of everyone we care for and, by making sure that our NHS services are smoke-free, we benefit the health of people who use our services as well as the health of the people who work for us.