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At West Herts we recognise the importance of a good work life balance and the ability to work flexibly.
Job summaryBand 5/6 depending on skills and experience.
This is a fixed term full-time post which is open to qualified nurses who wish to pursue a career in clinical research.
The post holder will undertake a competency-based program working with established multidisciplinary research teams across a variety of disciplines.
The training includes study sessions which are combined with practice placements to deliver an integrated approach to clinical research training. The post is funded by the Local Research Network.
Main duties of the job
Clinical activities to be performed under supervision and with increasing level of autonomy throughout the training period:
Attend multidisciplinary team meetings, helping to identify patients eligible for clinical trials.
Assist with recruitment of patients to clinical trials using trial eligibility criteria.
Assist in the smooth running of clinics by obtaining results and x-rays/scans to be seen prior to patients' appointments.
Book investigations as directed by medical and nursing staff and data managers.
Assist patients with quality of life and other questionnaires as necessary.
Deal with telephone queries from patients and their carers with the support of the research nurse. Refer queries to other to another member of the multidisciplinary team as required.
Be involved in the administration of experimental and/or unlicensed intravenous investigational medicinal products.
Perform phlebotomy.
Assist in the safe handling, storage and shipping of bloods, histology specimens and other body fluids required for research purposes.
Learn to become the patient's guide and advocate through the complex decision-making process involved in considering participation in trials. Enable patients to articulate reasons for trial participation or refusal.
Learn how to communicate sensitive disease and diagnostic information and be able to deal with the emotional impact of bad news.
About us
There has never been a more exciting time to join West Hertfordshire Teaching Hospitals NHS Trust!
Major redevelopment works are planned as part of the New Hospital Programme. These will be most dramatic at Watford General Hospital where up to 90% of buildings will be new.
The trust has recently gained 'teaching hospital' status which reflects the dedicated work of many teams and individuals who have set the standard for delivering high quality training, learning and education at all levels of the workforce.
We are a flexible working employer
At West Herts we recognise the importance of a good work life balance and the ability to work flexibly. We are delighted to offer a variety of flexible working options for all staff. Please check out our web page for more information.
www.jobsincare.com/job/jBnxpet1
We encourage and welcome people with disabilities. If you need help, please ask.
We reserve the right to close this advert early due to the volume of applicants. Please apply as soon as possible to avoid disappointment.
Job description
Job responsibilities
Research administration skills to be developed during the training period:
Understand international, national, and local policies and legislation relating to clinical trials.
Learn to prepare for external inspections (eg MHRA) and internal audits.
Register/randomise patients into trial protocols.
Learn to extract clinical data from patients casenotes and transfer the data into the trial Case Report Forms.
Assist in accurate and complete data collection, updating and maintenance of databasesand computerised systems.
Take responsibility for filing and safe storage of clinical trials data sheets and for sending to Clinical Trials Units as appropriate.
Help to manage and facilitate clinical trials, establishing and maintaining channels of communication amongst staff and departments to ensure policies and protocols are understood and adhered to.
Understand the role of clinical trials units and liaise with units as necessary.
Assist in the preparation of research proposals for submission to the Local Ethics Committee and R&D department.
Attend and participate in unit meetings and seminars.
Job description
Job responsibilities
Research administration skills to be developed during the training period:
Understand international, national, and local policies and legislation relating to clinical trials.
Learn to prepare for external inspections (eg MHRA) and internal audits.
Register/randomise patients into trial protocols.
Learn to extract clinical data from patients casenotes and transfer the data into the trial Case Report Forms.
Assist in accurate and complete data collection, updating and maintenance of databasesand computerised systems.
Take responsibility for filing and safe storage of clinical trials data sheets and for sending to Clinical Trials Units as appropriate.
Help to manage and facilitate clinical trials, establishing and maintaining channels of communication amongst staff and departments to ensure policies and protocols are understood and adhered to.
Understand the role of clinical trials units and liaise with units as necessary.
Assist in the preparation of research proposals for submission to the Local Ethics Committee and R&D department.
Attend and participate in unit meetings and seminars.
Person Specification
Education and qualifications
Essential
- Registered Nurse Graduate qualification with NMC registration
- GCP trained with understanding of Research Governance procedures/ ICH-GCP.
Essential
- A keen interest in research
- Understanding of research networks and clinical trials processes.
Essential
- Post registration experience of working within the NHS in an acute or research setting
- Experience of teaching, supervising and mentoring junior staff.
Essential
- Basic computer skills, proficient in Microsoft Office, Word, Excel, Access and Outlook.
- Able to use own initiative, innovate and respond to change
- Phlebotomy and cannulation
Essential
- Adaptable and flexible
- Able to work in a team
- Self-motivated
- Excellent interpersonal skills
- Capable of working effectively within multidisciplinary teams.
Education and qualifications
Essential
- Registered Nurse Graduate qualification with NMC registration
- GCP trained with understanding of Research Governance procedures/ ICH-GCP.
Essential
- A keen interest in research
- Understanding of research networks and clinical trials processes.
Essential
- Post registration experience of working within the NHS in an acute or research setting
- Experience of teaching, supervising and mentoring junior staff.
Essential
- Basic computer skills, proficient in Microsoft Office, Word, Excel, Access and Outlook.
- Able to use own initiative, innovate and respond to change
- Phlebotomy and cannulation
Essential
- Adaptable and flexible
- Able to work in a team
- Self-motivated
- Excellent interpersonal skills
- Capable of working effectively within multidisciplinary teams.
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.
Certificate of Sponsorship
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 .
From 6 April 2, 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. .
UK Registration
Applicants must have current UK professional registration. For further information please see
Additional information
Certificate of Sponsorship
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 .
From 6 April 2, 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. .
UK Registration
Applicants must have current UK professional registration. For further information please see
Employer details
Employer name
West Hertfordshire Teaching Hospitals NHS Trust
Address
Cross Site
Watford
WD18 0HB
Employer's website
Job summary
Band 5/6 depending on skills and experience.
This is a fixed term full-time post which is open to qualified nurses who wish to pursue a career in clinical research.
The post holder will undertake a competency-based program working with established multidisciplinary research teams across a variety of disciplines.
The training includes study sessions which are combined with practice placements to deliver an integrated approach to clinical research training. The post is funded by the Local Research Network.
Main duties of the job
Clinical activities to be performed under supervision and with increasing level of autonomy throughout the training period:
Attend multidisciplinary team meetings, helping to identify patients eligible for clinical trials.
Assist with recruitment of patients to clinical trials using trial eligibility criteria.
Assist in the smooth running of clinics by obtaining results and x-rays/scans to be seen prior to patients' appointments.
Book investigations as directed by medical and nursing staff and data managers.
Assist patients with quality of life and other questionnaires as necessary.
Deal with telephone queries from patients and their carers with the support of the research nurse. Refer queries to other to another member of the multidisciplinary team as required.
Be involved in the administration of experimental and/or unlicensed intravenous investigational medicinal products.
Perform phlebotomy.
Assist in the safe handling, storage and shipping of bloods, histology specimens and other body fluids required for research purposes.
Learn to become the patient's guide and advocate through the complex decision-making process involved in considering participation in trials. Enable patients to articulate reasons for trial participation or refusal.
Learn how to communicate sensitive disease and diagnostic information and be able to deal with the emotional impact of bad news.
About us
There has never been a more exciting time to join West Hertfordshire Teaching Hospitals NHS Trust!
Major redevelopment works are planned as part of the New Hospital Programme. These will be most dramatic at Watford General Hospital where up to 90% of buildings will be new.
The trust has recently gained 'teaching hospital' status which reflects the dedicated work of many teams and individuals who have set the standard for delivering high quality training, learning and education at all levels of the workforce.
We are a flexible working employer
At West Herts we recognise the importance of a good work life balance and the ability to work flexibly. We are delighted to offer a variety of flexible working options for all staff. Please check out our web page for more information.
www.jobsincare.com/job/jBnxpet1
We encourage and welcome people with disabilities. If you need help, please ask.
We reserve the right to close this advert early due to the volume of applicants. Please apply as soon as possible to avoid disappointment.
Job description
Job responsibilities
Research administration skills to be developed during the training period:
Understand international, national, and local policies and legislation relating to clinical trials.
Learn to prepare for external inspections (eg MHRA) and internal audits.
Register/randomise patients into trial protocols.
Learn to extract clinical data from patients casenotes and transfer the data into the trial Case Report Forms.
Assist in accurate and complete data collection, updating and maintenance of databasesand computerised systems.
Take responsibility for filing and safe storage of clinical trials data sheets and for sending to Clinical Trials Units as appropriate.
Help to manage and facilitate clinical trials, establishing and maintaining channels of communication amongst staff and departments to ensure policies and protocols are understood and adhered to.
Understand the role of clinical trials units and liaise with units as necessary.
Assist in the preparation of research proposals for submission to the Local Ethics Committee and R&D department.
Attend and participate in unit meetings and seminars.
Job description
Job responsibilities
Research administration skills to be developed during the training period:
Understand international, national, and local policies and legislation relating to clinical trials.
Learn to prepare for external inspections (eg MHRA) and internal audits.
Register/randomise patients into trial protocols.
Learn to extract clinical data from patients casenotes and transfer the data into the trial Case Report Forms.
Assist in accurate and complete data collection, updating and maintenance of databasesand computerised systems.
Take responsibility for filing and safe storage of clinical trials data sheets and for sending to Clinical Trials Units as appropriate.
Help to manage and facilitate clinical trials, establishing and maintaining channels of communication amongst staff and departments to ensure policies and protocols are understood and adhered to.
Understand the role of clinical trials units and liaise with units as necessary.
Assist in the preparation of research proposals for submission to the Local Ethics Committee and R&D department.
Attend and participate in unit meetings and seminars.
Person Specification
Education and qualifications
Essential
Essential
Essential
Essential
Essential
Education and qualifications
Essential
Essential
Essential
Essential
Essential
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.
Certificate of Sponsorship
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 .
From 6 April 2, 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. .
UK Registration
Applicants must have current UK professional registration. For further information please see
Additional information
Certificate of Sponsorship
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 .
From 6 April 2, 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. .
UK Registration
Applicants must have current UK professional registration. For further information please see
Employer details
Employer name
West Hertfordshire Teaching Hospitals NHS Trust
Address
Cross Site
Watford
WD18 0HB
Employer's website
Band 5/6 depending on skills and experience.
This is a fixed term full-time post which is open to qualified nurses who wish to pursue a career in clinical research.
The post holder will undertake a competency-based program working with established multidisciplinary research teams across a variety of disciplines.
The training includes study sessions which are combined with practice placements to deliver an integrated approach to clinical research training. The post is funded by the Local Research Network.
Main duties of the job
Clinical activities to be performed under supervision and with increasing level of autonomy throughout the training period:
Attend multidisciplinary team meetings, helping to identify patients eligible for clinical trials.
Assist with recruitment of patients to clinical trials using trial eligibility criteria.
Assist in the smooth running of clinics by obtaining results and x-rays/scans to be seen prior to patients' appointments.
Book investigations as directed by medical and nursing staff and data managers.
Assist patients with quality of life and other questionnaires as necessary.
Deal with telephone queries from patients and their carers with the support of the research nurse. Refer queries to other to another member of the multidisciplinary team as required.
Be involved in the administration of experimental and/or unlicensed intravenous investigational medicinal products.
Perform phlebotomy.
Assist in the safe handling, storage and shipping of bloods, histology specimens and other body fluids required for research purposes.
Learn to become the patient's guide and advocate through the complex decision-making process involved in considering participation in trials. Enable patients to articulate reasons for trial participation or refusal.
Learn how to communicate sensitive disease and diagnostic information and be able to deal with the emotional impact of bad news.
About us
There has never been a more exciting time to join West Hertfordshire Teaching Hospitals NHS Trust!
Major redevelopment works are planned as part of the New Hospital Programme. These will be most dramatic at Watford General Hospital where up to 90% of buildings will be new.
The trust has recently gained 'teaching hospital' status which reflects the dedicated work of many teams and individuals who have set the standard for delivering high quality training, learning and education at all levels of the workforce.
We are a flexible working employer
At West Herts we recognise the importance of a good work life balance and the ability to work flexibly. We are delighted to offer a variety of flexible working options for all staff. Please check out our web page for more information.
www.jobsincare.com/job/jBnxpet1
We encourage and welcome people with disabilities. If you need help, please ask.
We reserve the right to close this advert early due to the volume of applicants. Please apply as soon as possible to avoid disappointment.
Job description
Job responsibilities
Research administration skills to be developed during the training period:
Understand international, national, and local policies and legislation relating to clinical trials.
Learn to prepare for external inspections (eg MHRA) and internal audits.
Register/randomise patients into trial protocols.
Learn to extract clinical data from patients casenotes and transfer the data into the trial Case Report Forms.
Assist in accurate and complete data collection, updating and maintenance of databasesand computerised systems.
Take responsibility for filing and safe storage of clinical trials data sheets and for sending to Clinical Trials Units as appropriate.
Help to manage and facilitate clinical trials, establishing and maintaining channels of communication amongst staff and departments to ensure policies and protocols are understood and adhered to.
Understand the role of clinical trials units and liaise with units as necessary.
Assist in the preparation of research proposals for submission to the Local Ethics Committee and R&D department.
Attend and participate in unit meetings and seminars.
Job description
Job responsibilities
Research administration skills to be developed during the training period:
Understand international, national, and local policies and legislation relating to clinical trials.
Learn to prepare for external inspections (eg MHRA) and internal audits.
Register/randomise patients into trial protocols.
Learn to extract clinical data from patients casenotes and transfer the data into the trial Case Report Forms.
Assist in accurate and complete data collection, updating and maintenance of databasesand computerised systems.
Take responsibility for filing and safe storage of clinical trials data sheets and for sending to Clinical Trials Units as appropriate.
Help to manage and facilitate clinical trials, establishing and maintaining channels of communication amongst staff and departments to ensure policies and protocols are understood and adhered to.
Understand the role of clinical trials units and liaise with units as necessary.
Assist in the preparation of research proposals for submission to the Local Ethics Committee and R&D department.
Attend and participate in unit meetings and seminars.
Person Specification
Education and qualifications
Essential
- Registered Nurse Graduate qualification with NMC registration
- GCP trained with understanding of Research Governance procedures/ ICH-GCP.
Essential
- A keen interest in research
- Understanding of research networks and clinical trials processes.
Essential
- Post registration experience of working within the NHS in an acute or research setting
- Experience of teaching, supervising and mentoring junior staff.
Essential
- Basic computer skills, proficient in Microsoft Office, Word, Excel, Access and Outlook.
- Able to use own initiative, innovate and respond to change
- Phlebotomy and cannulation
Essential
- Adaptable and flexible
- Able to work in a team
- Self-motivated
- Excellent interpersonal skills
- Capable of working effectively within multidisciplinary teams.
Education and qualifications
Essential
- Registered Nurse Graduate qualification with NMC registration
- GCP trained with understanding of Research Governance procedures/ ICH-GCP.
Essential
- A keen interest in research
- Understanding of research networks and clinical trials processes.
Essential
- Post registration experience of working within the NHS in an acute or research setting
- Experience of teaching, supervising and mentoring junior staff.
Essential
- Basic computer skills, proficient in Microsoft Office, Word, Excel, Access and Outlook.
- Able to use own initiative, innovate and respond to change
- Phlebotomy and cannulation
Essential
- Adaptable and flexible
- Able to work in a team
- Self-motivated
- Excellent interpersonal skills
- Capable of working effectively within multidisciplinary teams.
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.
Certificate of Sponsorship
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 .
From 6 April 2, 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. .
UK Registration
Applicants must have current UK professional registration. For further information please see
Additional information
Certificate of Sponsorship
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 .
From 6 April 2, 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. .
UK Registration
Applicants must have current UK professional registration. For further information please see
Employer details
Employer name
West Hertfordshire Teaching Hospitals NHS Trust
Address
Cross Site
Watford
WD18 0HB
Employer's website
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