Translational Research Technician

University of Leicester; Leicester Forest East; Presencial; GBP 24 000 - 32 000; Tempo integral

Resumo da oferta

The University of Leicester’s Leicester ECMC seeks a Translational Research Technician to support tissue collection for clinical studies and early‑phase trials across Leicester hospital sites.

You will obtain consent, collect samples in operating theatres and clinics, and process them to GCLP standards, while helping to maintain facilities and train staff in tissue handling and storage.

Qualificações

• NVQ Level 3 or equivalent in a relevant subject (e.g. BTEC or ONC).
• Experience in a technical or clinical role involving human tissue samples.
• Understanding of regulatory requirements including Good Clinical Practice, The Human Tissue Act and health and laboratory safety standards.

Responsabilidades

• Support tissue collection activities for clinical research studies and early-phase trials across Leicester hospital sites.
• Obtain consent to research studies from patients and volunteers.
• Collect samples from operating theatres and clinics; process samples in accordance with GCLP standards and SOPs.
• Maintain laboratory facilities and monitor equipment.
• Support training for staff and students in tissue handling and storage.

Conhecimentos

Attention to detail

Organisational skills

Interpersonal skills

Teamwork

Flexibility

Formação académica

NVQ Level 3 or equivalent (BTEC/ONC)

Descrição da oferta de emprego

About the role

The Leicester Experimental Cancer Medicine Centre (ECMC) is part of a UK-wide network dedicated to advancing early-phase and translational cancer research. Working across the University of Leicester and University Hospitals of Leicester NHS Trust, the ECMC provides the infrastructure and expertise to deliver first-in-human trials and biomarker-driven studies. As a Translational Research Technician, you will play a vital role in supporting tissue collection activities for a range of clinical research studies and early-phase trials. This includes obtaining consent to research studies from patients and volunteers, collecting samples from operating theatres and clinics across Leicester hospital sites and processing of samples in accordance with Good Clinical Laboratory Practice (GCLP) standards and Standard operating procedures.

You will also contribute to maintaining laboratory facilities, monitoring equipment, and supporting training for staff and students in tissue handling and storage.

This position requires close collaboration with clinical teams and research colleagues to ensure timely collection of clinical specimens in compliance with regulatory requirements. You will be part of a dynamic environment where flexibility is key, as sample collections may occasionally be delayed or rescheduled.

Your work will directly support the ECMC’s mission to accelerate the development of new cancer treatments and diagnostics, making a real difference to patient care.

About you

You will hold a minimum of NVQ Level 3 (such as BTEC or ONC) in a relevant subject and have experience in a technical or clinical role involving human tissue samples. A sound understanding of regulatory requirements, including Good Clinical Practice, The Human Tissue Act and health and laboratory safety standards, is essential, along with excellent attention to detail and strong organisational skills.

You will be confident working in both clinical and laboratory settings, including operating theatres, and be able to work effectively both independently and as part of a team. You will demonstrate flexibility in responding to changing clinical demands and be willing to travel between hospital sites as required.

You will also possess excellent interpersonal and communication skills, with the ability to build effective working relationships and communicate confidently with a wide range of stakeholders, including patients, clinical teams, researchers, and laboratory staff.

Above all, you will share our values of inclusivity, collaboration and impact, and be motivated to contribute to research that improves outcomes for cancer patients.

Experience in an NHS or clinical research environment and experience in adhering to GCLP standards would be advantageous