Job summary
Clinical Trials Practitioner - Band 6
We are looking for a motivated CTP to work in the busy Cardiology Research Department. You will be tasked with the running of a variety of clinical trials, in accordance with good clinical practice guidelines, with particular emphasis on supporting the team in multicentre studies coordination.
We are the biggest cardiovascular centre in Europe and have a growing portfolio of interventional research for cardiac patients. The post is for a one-year fixed term contract position in the first instance with possibility of extension.
For informal enquiries or to arrange a visit please contact:
Mervyn Andiapen, Research Manager.Email: mervyn.andiapen@nhs.net
Main duties of the job
The primary responsibility for this post holder is to take a leading role in the setting up and running of a portfolio of cardiology research, initiate and manage different projects within the department.
You will be a CTP with a strong background in clinical trials management. You must demonstrate strong organisational, interpersonal and communication skills, be computer literate, flexible and be able to manage your own time effectively. Excellent time management and IT skills are essential to the role. Experience of formal and informal teaching and clinical research will be advantageous.
About us
Barts Health is one of the largest NHS trusts in the country, and one of Britain's leading healthcare providers.
The Barts Health group of NHS hospitals is entering an exciting new era on our improvement journey to becoming an outstanding organisation with a world-class clinical reputation. Having lifted ourselves out of special measures, we now have the impetus and breathing space to chart a fresh course in which we are continually striving to improve all our services for patients.
Our vision is to be a high-performing group of NHS hospitals, renowned for excellence and innovation, and providing safe and compassionate care to our patients in east London and beyond. That means being a provider of excellent patient safety, known for delivering consistently high standards of harm-free care and always caring for patients in the right place at the right time. It also means being an outstanding place to work, in which our WeCare values and behaviours are visible to all and guide us in how we work together.
We strive to live by our WeCare values and are committed to promoting inclusion, where every staff member has a sense of belonging. We value our differences and fully advocate, cultivate and support an inclusive working environment.
Job description
Job responsibilities
The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below.
Job description
Job responsibilities
The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below.
Person Specification
Qualifications
Essential
- -Possession of an undergraduate degree in Nursing, Science or Health related discipline
Desirable
- -Research qualification
- -Good Clinical Practice certification
- -ALS/ILS or equivalent
- -Registered Nurse with current NMC registration
- -Intravenous accreditation
- -Teaching/mentorship course or equivalent
Experience
Essential
- -Clinical Trials and Project management experience
- -Experience of clinical trial data entry on multiple platforms
- -Experience in clinical, organisational and team management
- -Experience of working as part of a multidisciplinary team
- -Experience of explaining complex concepts to colleagues, patients in a clear and simplified manner
- -Experience of formal & informal teaching of patients and staff
- -Experience of managing physically and emotionally challenging patient cohorts and environments
Desirable
- -Experience in research nursing in clinical investigations or trials
- -Experience in cardiology or cardiac/critical care environment for at least 1 year
Knowledge
Essential
- -Evidence of continuous personal development
- -Knowledge and experience of Research Governance, EU Clinical Trials Directive and Good Clinical Practice
- -Knowledge of Trials Research Management Software e.g EDGE
- -Clinical Trials Experience
Desirable
- -Demonstrate an understanding of national research networks.
- -Basic statistical knowledge
Skills
Essential
- -Proactive and self-motivated with ability to lead, motivate and empower others.
- -Well-developed interpersonal and communication skills including: interpersonal, liaison and negotiating skills.
- - Ability to confront challenging issues taking a problem-solving approach.
- - Ability to produce clear, accurate written and verbal reports.
- - Ability to prioritise, meet tight deadlines and work independently on a number of projects
- -Ability to work in a multi-professional arena
- -Attention to detail and meticulous, accurate documentation
- -Computer Literacy
Desirable
- -Ability to lead and manage meetings effectively.
- - Has some budgetary and resources management skills
- - Phlebotomy and cannulation skills
Other
Essential
- -Willingness to work flexible hours on occasion
- - Displays enthusiastic and proactive approach to work
- - Enthusiasm for and desire to embed research in clinical practice
- - Able to articulate reason
Person Specification
Qualifications
Essential
- -Possession of an undergraduate degree in Nursing, Science or Health related discipline
Desirable
- -Research qualification
- -Good Clinical Practice certification
- -ALS/ILS or equivalent
- -Registered Nurse with current NMC registration
- -Intravenous accreditation
- -Teaching/mentorship course or equivalent
Experience
Essential
- -Clinical Trials and Project management experience
- -Experience of clinical trial data entry on multiple platforms
- -Experience in clinical, organisational and team management
- -Experience of working as part of a multidisciplinary team
- -Experience of explaining complex concepts to colleagues, patients in a clear and simplified manner
- -Experience of formal & informal teaching of patients and staff
- -Experience of managing physically and emotionally challenging patient cohorts and environments
Desirable
- -Experience in research nursing in clinical investigations or trials
- -Experience in cardiology or cardiac/critical care environment for at least 1 year
Knowledge
Essential
- -Evidence of continuous personal development
- -Knowledge and experience of Research Governance, EU Clinical Trials Directive and Good Clinical Practice
- -Knowledge of Trials Research Management Software e.g EDGE
- -Clinical Trials Experience
Desirable
- -Demonstrate an understanding of national research networks.
- -Basic statistical knowledge
Skills
Essential
- -Proactive and self-motivated with ability to lead, motivate and empower others.
- -Well-developed interpersonal and communication skills including: interpersonal, liaison and negotiating skills.
- - Ability to confront challenging issues taking a problem-solving approach.
- - Ability to produce clear, accurate written and verbal reports.
- - Ability to prioritise, meet tight deadlines and work independently on a number of projects
- -Ability to work in a multi-professional arena
- -Attention to detail and meticulous, accurate documentation
- -Computer Literacy
Desirable
- -Ability to lead and manage meetings effectively.
- - Has some budgetary and resources management skills
- - Phlebotomy and cannulation skills
Other
Essential
- -Willingness to work flexible hours on occasion
- - Displays enthusiastic and proactive approach to work
- - Enthusiasm for and desire to embed research in clinical practice
- - Able to articulate reason
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).
