Job summary
An exciting opportunity has arisen for a Band 6 Research Trials Practitioner to join the Centre of Medical Imaging (CMI) Research Team. Are you dynamic, patient centred and looking for an exciting challenge? Why not consider joining our team at UCLH.The role is a combination of clinical and research responsibilities. You will be a point of contact for study Principal Investigators, sponsors & patients across UCLH sites. This means effective communication and team working skills are essential.
You will be involved in ensuring that research undertaken safeguards the well-being of patients and is undertaken within Good Clinical Practice (GCP) Guidelines.
Main duties of the job
o Responding to enquiries from potential participantso Pre-screening potential participants by phone and arranging screening visitso Obtain informed consent and conduct screeningo Arrange and attend MRI scans and other clinic visits across UCLH sites.o Be a point of contact for trial participantso Complete trial forms and prompt data entry to the online databaseso Manage and facilitate participant visits.
About us
University College London Hospitals NHS Foundation Trust (UCLH) is one of the most complex NHS trusts in the UK, serving a large and diverse population. We provide academically led acute and specialist services, to people from the local area, from throughout the United Kingdom and overseas. Our vision is to deliver top-quality patient care, excellent education, and world-class research.
We provide first-class acute and specialist services across eight sites:
University College Hospital (incorporating the Elizabeth Garrett Anderson Wing)
National Hospital for Neurology and Neurosurgery
Royal National ENT and Eastman Dental Hospitals
University College Hospital Grafton Way Building
Royal London Hospital for Integrated Medicine
University College Hospital Macmillan Cancer Centre
The Hospital for Tropical Diseases
University College Hospital at Westmoreland Street
We are dedicated to the diagnosis and treatment of many complex illnesses. UCLH specialises in women's health and the treatment of cancer, infection, neurological, gastrointestinal and oral disease. It has world class support services including critical care, imaging, nuclear medicine and pathology.
Job description
Job responsibilities
For the full Person Specification and more information regarding the main responsibilities of this role, please refer to the attached Job Description.
Come and be a part of the best NHS trust in England to work for, according to our staff*
* UCLH top trust to work at in England - In the most recent NHS staff survey UCLH had the highest percentage of staff who said they would recommend us as a place to work, out of all general acute or acute/community NHS trusts in England for the third year in a row.
UCLH recognises the benefits of flexible working for staff To find out more, visit: Flexible working.
To discover more about what makes UCLH a great place to work, visit: Why Choose UCLH?
Job description
Job responsibilities
For the full Person Specification and more information regarding the main responsibilities of this role, please refer to the attached Job Description.
Come and be a part of the best NHS trust in England to work for, according to our staff*
* UCLH top trust to work at in England - In the most recent NHS staff survey UCLH had the highest percentage of staff who said they would recommend us as a place to work, out of all general acute or acute/community NHS trusts in England for the third year in a row.
UCLH recognises the benefits of flexible working for staff To find out more, visit: Flexible working.
To discover more about what makes UCLH a great place to work, visit: Why Choose UCLH?
Person Specification
Knowledge and Qualifications
Essential
- Science related degree or significant experience of working in research in the NHS
- Knowledge of research design and methods
- Knowledge of health management
- Knowledge of Research Governance Framework, EU Clinical Trials Directives
Experience
Essential
- Experience of working under minimal supervision
- Experience of managing and developing databases and spreadsheets
- Experience of working in clinical trial environment
- Experience of working to deadlines
- Practical experience of monitoring clinical trial activity
- Experience of dealing with confidential information
- Experience of working in a health care setting or research environment, including clinical trials
- Experience of dealing with the public in person and on the phone
- Experience of working as part of a team and collaboratively across multi professional teams
Desirable
- Experience of carrying out clinical research project from study start up to close out
Skills and Abilities
Essential
- Proven ability to work under own initiative
- Excellent interpersonal skills with an ability to develop and maintain constructive relationships with professional, managerial and multi-disciplinary groups.
- Able to communicate effectively verbally and in writing and electronically, with a range of people on a range of matters including staff, patients and relatives, tailored
- Proven ability to work as part of a team with the ability to work autonomously when required
- Computer literacy to include experience of Word and Excel and use of research databases
- Evidence of working in line with good clinical practice guidelines (GCP), understanding of research governance, EU Clinical Trials Directive.
Desirable
- Enthusiasm for learning, new ideas and continuing professional development
- Enthusiasm for learning, new ideas and continuing professional development
- Ability to support others
Communication
Essential
- Excellent interpersonal & communication skills with the ability to deal effectively with a wide range of people (e.g., medical & nursing staff, managers, admin staff) in a helpful manner.
Responsibilities towards promoting Equality Diversity and Inclusion
Essential
- Demonstratable understanding of the Equality, Diversity, and Inclusion and/or Knowledge of the NHS obligations under the Equality Act 2010 and the Public Sector Equality Duties
Specific Requirements
Essential
- Meticulous in approach to work and record-keeping
- Excellent interpersonal skills with a proven track record of communicating with a range of stakeholders from academia and commerce, at all levels of seniority.
Desirable
- Experience of using research related database/network including EDGE, Clinical Governance and CPMS.
- Experience of using electronic patient record systems including EPIC
Person Specification
Knowledge and Qualifications
Essential
- Science related degree or significant experience of working in research in the NHS
- Knowledge of research design and methods
- Knowledge of health management
- Knowledge of Research Governance Framework, EU Clinical Trials Directives
Experience
Essential
- Experience of working under minimal supervision
- Experience of managing and developing databases and spreadsheets
- Experience of working in clinical trial environment
- Experience of working to deadlines
- Practical experience of monitoring clinical trial activity
- Experience of dealing with confidential information
- Experience of working in a health care setting or research environment, including clinical trials
- Experience of dealing with the public in person and on the phone
- Experience of working as part of a team and collaboratively across multi professional teams
Desirable
- Experience of carrying out clinical research project from study start up to close out
Skills and Abilities
Essential
- Proven ability to work under own initiative
- Excellent interpersonal skills with an ability to develop and maintain constructive relationships with professional, managerial and multi-disciplinary groups.
- Able to communicate effectively verbally and in writing and electronically, with a range of people on a range of matters including staff, patients and relatives, tailored
- Proven ability to work as part of a team with the ability to work autonomously when required
- Computer literacy to include experience of Word and Excel and use of research databases
- Evidence of working in line with good clinical practice guidelines (GCP), understanding of research governance, EU Clinical Trials Directive.
Desirable
- Enthusiasm for learning, new ideas and continuing professional development
- Enthusiasm for learning, new ideas and continuing professional development
- Ability to support others
Communication
Essential
- Excellent interpersonal & communication skills with the ability to deal effectively with a wide range of people (e.g., medical & nursing staff, managers, admin staff) in a helpful manner.
Responsibilities towards promoting Equality Diversity and Inclusion
Essential
- Demonstratable understanding of the Equality, Diversity, and Inclusion and/or Knowledge of the NHS obligations under the Equality Act 2010 and the Public Sector Equality Duties
Specific Requirements
Essential
- Meticulous in approach to work and record-keeping
- Excellent interpersonal skills with a proven track record of communicating with a range of stakeholders from academia and commerce, at all levels of seniority.
Desirable
- Experience of using research related database/network including EDGE, Clinical Governance and CPMS.
- Experience of using electronic patient record systems including EPIC
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Employer details
Employer name
University College London Hospitals NHS Foundation Trust
Address
University College London Hospital
250 Euston Road
London
NW1 2PG
Employer's website
https://www.uclh.nhs.uk (Opens in a new tab)
