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East London NHS Foundation Trust; Luton; On-site; GBP 28,000 - 36,000; Full time

Job summary

East London NHS Foundation Trust is seeking a Clinical Studies Assistant/Research Nurse to support a range of NHS studies. You will work with clinical teams to recruit service users, obtain informed consent, and conduct baseline assessments in line with GCP.

The role involves on-site presence and careful data management across multiple studies. You will contribute to study setup, maintain site files, and promote a research culture within the Trust, helping ensure timely delivery of study

Qualifications

• Experience in obtaining informed consent and coordinating participant recruitment.
• Ability to collect, manage, and input study data accurately.
• Understanding of Good Clinical Practice (GCP) principles in NHS research.
• Strong communication with clinical teams and study participants.

Responsibilities

• Identify, screen, and recruit participants into multiple studies per protocol.
• Obtain informed consent following GCP guidelines and document appropriately.
• Assist with baseline assessments and data collection per study protocol.
• Maintain trial site files and delegation logs, ensuring governance compliance.
• Support study setup and collaborate with clinical services during launches.
• Promote research culture among clinicians and service users.

Skills

Consent and recruitment

Data collection

GCP knowledge

Communication with clinicians

Participant liaison

Tools

EDGE Data Entry System

Job description

Clinical Studies Assistant/Research nurse | East London NHS Foundation Trust

Company: East London NHS Foundation Trust

The research delivery workforce is a vital resource; their skills and expertise ensure that patients and the economy benefit from a vibrant research culture as an integral part of health and care for all. The research delivery team are involved in a range of activities, including:

• Seeking ongoing informed consent as a voluntary agreement with research study participants, ensuring their understanding of the research and its risks
• Identification, screening, and randomisation of research study participants
• Ensuring high quality data input at source and its management through a research workflow

Clinical Studies Assistants are a core part of the research delivery workforce that specialise in consent, data collection, and other study protocol activities. This is a varied role involving work across multiple studies, services, and teams. Postholders will be expected tospend a minimum of 40% of time on site, either across services or at their designated base.

The post-holder will be responsible for liaising with busy clinicians, identifying and recruiting service users into a portfolio of studies to meet targets within agreed timelines, conducting baseline assessments, and maintaining accurate site files and case report files. They will also provide additional support to study teams when necessary and actively promote research among clinicians, service users, and the wider NHS community.

This is a patient facing role and will require the post-holder to be in-person 4 days a week.

The purpose of this post is to increase the number of people participating in research studies ELFT, by:

• Assisting clinical teams and NHS services in identifying and recruiting participants in research studies, including service users, carers, and staff
• Providing information and support for patients, carers and staff enrolling in research projects
• Facilitating delivery of study procedures in line with the study protocol, performing baseline assessments of study participants
• Assisting the efficient set up and delivery of studies within ELFT, thus contributing to the performance metrics set for the Trust by the Regional RDN.

Contributing to the development of a culture within the Trust where research is actively promoted at all levels.

Our mission is to make a positive difference to people's lives by improving the quality of life for all we serve. Our values are: We Care, We Respect, We are Inclusive – so we are looking for people who live and breathe these qualities when supporting service users and carers, and in their relationships with colleagues in the Trust and our partner organisations.

Research Context

• Demonstrate a comprehensive understanding of the portfolio of studies taking place in the Trust.
• Demonstrate a practical understanding of how the principles of Good Clinical Practice (GCP) are implemented using everyday examples of their working practice.
• Be able to discusses their individual contribution to delivering research in the NHS and understand the role of their colleagues.
• Be able to identify different study types (e.g., interventional, observation) and design (e.g., randomised, double-blind) and explain what these terms mean.
• Monitor compliance with governance requirements and promptly report any non-compliance issues to line manager.

Study set-up

• Establish trial site files compliant with research governance and GCP requirements.
• Assists in the organisation of trial documentation for study set-up.
• Contribute to feasibility assessments under supervision.
• Demonstrate a broad awareness of the approvals required to conduct research in the NHS studies and the processes by which these approvals are obtained.
• Completes the delegation log for a new trial & demonstrates understanding of delegated duties.
• Assist in identifying suitable clinical services, wards, or departments for participant recruitment.
• Under supervision, collaborate with clinical services during the study set-up phase.
• As required, attend site initiation visits with the Principal Investigator, research team and clinical staff to ensure effective study launch and protocol understanding.
• Liaise with clinical teams to promote research studies and ensure appropriate referrals and recruitment of participants.
• Identify, screen, and recruit participants in line with protocol-defined inclusion and exclusion criteria, adhering to national and local approvals.
• Clearly explain studies to service users, address their questions, and obtain informed consent in accordance with GCP principles.
• Provide comprehensive information about studies to service users, and where appropriate extending this information to families, and treating clinicians to ensure informed decision-making.
• Where appropriate apply capacity assessment at consent and baseline visit.
• Proactively seeks documentation to confirm informed consent has been provided by the participant; and Identifies errors/concerns in documents.
• Undertakes collection of biological samples (including blood & phlebotomy) in line with local & national regulations
• Facilitate delivery of baseline measures in line with the study protocol e.g. psychological assessments.
• Contribute to the collection and reporting of local recruitment data by maintaining updated screening and recruitment logs as required.
• Regularly monitor and report study recruitment progress, identify areas of low recruitment, and work with line manager to implement strategies for improvement.
• Contribute to the development of policies and standard operating procedures (SOPs) to support adherence to protocols.

Data Management

• Collect, collate, and manage research data in strict adherence to study protocols, ensuring accuracy and completeness.
• Establish and/or maintain in-house and sponsor documentation systems and accurate study contacts.
• Creates and maintains research files according to standard operating procedures (SOPs); demonstrates an ability to manage version control of study documents.
• Maintain meticulous and accurate patient records, ensuring all relevant study information is documented in medical notes and source documentation; identify and seek to correct incomplete, inaccurate, or misleading documentation or data entry.
• Undertake the accurate and complete collection of data, and insertion of data into case report forms (CRFs) and other study-related documentation; identify errors and inconsistencies between CRFs and source data and seek to resolve these.
• Ensure that all data collection and storage meet the requirements of study protocols, research governance, and data protection legislation.
• Facilitate accurate and timely recording of patient recruitment data using the EDGE Data Entry System.
• Has a robust understanding of what constitutes a data breach/ confidentiality breach and raises concerns when processes to ensure confidentiality are not adhered to.
• Prepare documents and facilities for monitoring visits and work with the study monitor during visit; respond to auditing and monitoring recommendations.
• Contributes to study closure and preparation of documents for archiving, liaising with the sponsor and R&I department.
• Articulates their own responsibilities and recognises the boundary of their own role and when to refer to others.
• Raise concerns and report instances of suspected protocol deviation.
• Identify and elevate patient risks to the appropriate care team during study visits, ensuring timely intervention.
• Record and report incidents of harm or near misses in line with the Trust’s incident reporting policies, including timely and appropriate referral.
• Prepares initial and follow-up adverse event reports in liaison with clinical staff.

This advert closes on Thursday 1 Oct 2026

East of England Community Health & Care NHS Trust