Job summary
An exciting opportunity has arisen for a Research Nurse/ Practitioner to work within the Research Team on our commercial and academic Haematology/ Oncology trial portfolio. We are seeking a highly motivated person to join our friendly team, this post would suit a secondment allowing the post holder to gain more experience in the field of clinical research.
We have an increasing portfolio of Hematological trials including commercially sponsored trials working with Industry Partners. The job would give direct patient contact, advocating for patients and enabling them to participate in clinical research.
The United Lincolnshire Hospitals NHS Trust works in partnership with the regional NHS Trusts and Universities and has been successful in establishing and hosting East Midlands Clinical Research Network (CRNEM) staff to support clinical research.
Main duties of the job
The successful applicant will be expected to work on a variety of clinical trials with the senior research nurse. The post is focused on the Hematological trial portfolio and will include working alongside Consultants and Clinical teams at Pilgrim Hospital Boston.
We are looking for an enthusiastic and motivated Registered Nurse or Allied Health Professional with excellent organisational, communication and effective time management skills with the ability to work on their own initiative and as part of a team. Previous experience of clinical trials/research is desirable but not essential. This post would be appropriate for a secondment to gain high quality experience of working on clinical research trials.
This is an excellent opportunity to work with patients and clinicians enabling the people in Lincolnshire to participate in research and to improve and develop evidence based healthcare.
About us
The post holder is expected to treat patients, service users and carers with courtesy, care and compassion at all times, treating each person as an individual by offering a personalised service. United Lincolnshire Hospitals NHS Trust staff will adopt behaviours and attitudes, which promote, supports and respects privacy and dignity in accordance with the Trust Dignity policies and dignity in care pledges.
We are a friendly research team and are keen to support and nurture our staff enabling us to provide the very best care and be involved in the creation of the best evidence based care.
Job description
Job responsibilities
To play an active role in the recruitment of patients into clinical trials and studies. To provide patients with appropriate information about relevant trials and to ensure that patients understand their disease and treatment options to enable them to make an informed decision regarding participation.To report Adverse Events using appropriate procedures, as defined by the trial protocol and GCP, including the expedited reporting of Serious Adverse Events and Suspected Unexpected Serious Adverse Reactions.Accurate data collection and record keeping, including medication accountability, case report forms, patient information and patient health records. In addition to perform clinical trial procedures e.g. venepuncture, obtaining trial specific biological samples, ECGs, BP monitoring, height & weight recording.To act as a contact point and a resource to patients both during the trial and in the follow-up phase.To communicate and liaise regularly with colleagues within the trust and wider health care system, to include the Principle Investigator, Sponsor and CRN East Midlands team.Liaise with medical, nursing and allied health professionals to ensure that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and relevant legislative/EU Clinical Trials guidance and departmental Standard Operating Procedures (SOPS).Have the ability to appropriately delegate duties under the oversight of the senior research Nurse where required.Any other duties as identified by the line manager.Being responsible for continuing professional development and training needs with support from the line manager. Attending any study specific training and meetings as required. Participate in regular Wellbeing meetings and an Annual Appraisal to identify personal and professional objectives and development needs.
Job description
Job responsibilities
To play an active role in the recruitment of patients into clinical trials and studies. To provide patients with appropriate information about relevant trials and to ensure that patients understand their disease and treatment options to enable them to make an informed decision regarding participation.To report Adverse Events using appropriate procedures, as defined by the trial protocol and GCP, including the expedited reporting of Serious Adverse Events and Suspected Unexpected Serious Adverse Reactions.Accurate data collection and record keeping, including medication accountability, case report forms, patient information and patient health records. In addition to perform clinical trial procedures e.g. venepuncture, obtaining trial specific biological samples, ECGs, BP monitoring, height & weight recording.To act as a contact point and a resource to patients both during the trial and in the follow-up phase.To communicate and liaise regularly with colleagues within the trust and wider health care system, to include the Principle Investigator, Sponsor and CRN East Midlands team.Liaise with medical, nursing and allied health professionals to ensure that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and relevant legislative/EU Clinical Trials guidance and departmental Standard Operating Procedures (SOPS).Have the ability to appropriately delegate duties under the oversight of the senior research Nurse where required.Any other duties as identified by the line manager.Being responsible for continuing professional development and training needs with support from the line manager. Attending any study specific training and meetings as required. Participate in regular Wellbeing meetings and an Annual Appraisal to identify personal and professional objectives and development needs.
Person Specification
Qualifications
Essential
- Registered nurse with current valid NMC pin or Allied Health Professional with professional registration or Research Practitioner Registration or willingness to work towards.
Desirable
- Degree level Qualification or willingness to work towards.
Knowledge and Experience
Essential
- Knowledge and experience within the clinical setting of Haematology/ Oncology
- Knowledge or experience of local, national or international research being undertaken.
- Knowledge of the issue related to clinical data management, confidentiality and GDPR
Desirable
- Experience of venipuncture and handling of biological samples.
- Experience of working in a clinical research team.
Evidence of Particular Knowledge, Skills, and Aptitudes
Essential
- Ability to work autonomously using own initiative and as a member of a team.
- High level of interpersonal, written and verbal skills, engaging with colleagues at all levels of the organisation.
- Ability to interpret complex trial protocols and communicate information. to professionals and laypersons having accuracy and attention to detail
- Excellent organisational skills with the ability to organise, prioritise and delegate work load.
- Ability to innovate and respond to change.
- Commitment to ongoing personal and professional development.
Desirable
- Ability to use word processing, spread sheets and databases to an intermediate level
Person Specification
Qualifications
Essential
- Registered nurse with current valid NMC pin or Allied Health Professional with professional registration or Research Practitioner Registration or willingness to work towards.
Desirable
- Degree level Qualification or willingness to work towards.
Knowledge and Experience
Essential
- Knowledge and experience within the clinical setting of Haematology/ Oncology
- Knowledge or experience of local, national or international research being undertaken.
- Knowledge of the issue related to clinical data management, confidentiality and GDPR
Desirable
- Experience of venipuncture and handling of biological samples.
- Experience of working in a clinical research team.
Evidence of Particular Knowledge, Skills, and Aptitudes
Essential
- Ability to work autonomously using own initiative and as a member of a team.
- High level of interpersonal, written and verbal skills, engaging with colleagues at all levels of the organisation.
- Ability to interpret complex trial protocols and communicate information. to professionals and laypersons having accuracy and attention to detail
- Excellent organisational skills with the ability to organise, prioritise and delegate work load.
- Ability to innovate and respond to change.
- Commitment to ongoing personal and professional development.
Desirable
- Ability to use word processing, spread sheets and databases to an intermediate level
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).
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
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).
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
