Job summary
An exciting role within the award-winning Research Team at Surrey and Borders Partnership NHS Foundation Trust.
The primary role of the research nurse is to support a portfolio of mental health and dementia clinical trials across the Trust. You will be responsible for assessing and managing the care pathways for people who use our services and carers participating in clinical trials, be directly involved in the recruitment, education and monitoring of trial participants, collecting and preparing biological samples as per protocol and in the collection and documentation of accurate data.It would be advantageous that the post holder has experience in clinical skills such as phlebotomy and medication administration. Experience in neuro-psychometric evaluation of mental health would also be beneficial.We are committed to developing our staff in line with our Trust visions and values. There are many opportunities for personal and professional growth, ranging from clinical courses and programmes to development of clinical excellence and leadership skills.
The post holder will actively promote research amongst clinicians, service users and the wider NHS.
The post holder will be predominantly based at Two Bridges, Chertsey, but will be expected to attend events and meetings across the Trust's catchment area.
Main duties of the job
Key Responsibilitieso Work autonomously and assist in the management of a caseload of clinical trial participants whilst working as part of a multi-disciplinary team.o Identify suitable people who use our services for entry into clinical trialso Maintain accurate documentation of participants events in progress noteso Provide ongoing information, education and support to participants (and their significant others) regarding clinical trials and specific trial treatmentso Ensure that trial specific investigations are undertaken as required by the trial protocol and obtain results in order to establish eligibility and safety to enter the trialo Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial
- Phlebotomy and cannulation training, up to date IV drugs/ IV therapy administration competencyo Monitor treatment toxicity/side effects and initiate changes to treatment or treatment cessation as required by trial protocolso Report and record adverse events which occur whilst patients are under trial therapy to the trial co-ordinator/Principal Investigator and relevant local and regulatory authoritieso Act as a primary contact point for the trial participanto Maintain accurate participants trial documentation, complete Case Report Forms, including the use of electronic data capture systems and ensure relevant information is recorded in participants case notes
About us
Surrey and Borders Partnership NHS Foundation Trust is the leading provider of mental health, learning disability, neurodevelopmental and drug and alcohol services in Surrey and North East Hampshire. We support people of all ages and are passionate about providing high quality care that is delivered at the right time as close to home as possible to help people recover and stay well.
We are one of the top 10 mental Health, Learning Disability and Community Trust to work for nationwide. Our Trust is an inclusive and supportive employer that offers a wide range of staff networks, flexible working, free parking and excellent health and wellbeing support. We also provide a wide range of opportunities to help staff develop and progress.
Surrey is a beautiful county lying just 30 minutes away from Central London and from the South Coast. Our historic market towns and bustling districts are enveloped in wonderful countryside, and our excellent road and rail networks bring the rest of the country within easy reach. For international travel, both Gatwick and Heathrow airports are nearby.
Please note that we reserve the right to close posts as soon as sufficient applications are received.
We look forward to receiving your application!
Job description
Job responsibilities
- Experience required Minimum 2 years post qualification experience Working in the NHS Research experience desirableSuitable for someone who is: Self-motivated, flexible and able to adapt to changing demands, able to process information and interpret accordingly, able to organise own workload and prioritise work as it comes into the department, able to remain calm and professional under pressure and able to respect confidentiality guidelinesKey ResponsibilitiesClinical Work autonomously and assist in the management of a caseload of clinical trial participants whilst working as part of a multi-disciplinary team. Maintain effective communication with people who use our services, carers and professionals to ensure high quality service delivery Identify suitable people who use our services for entry into clinical trials Maintain accurate documentation of participants events in progress notes Ensure people who use our services are fully informed prior to entry into clinical trial programmes Provide ongoing information, education and support to participants (and their significant others) regarding clinical trials and specific trial treatments Ensure that trial specific investigations are undertaken as required by the trial protocol and obtain results in order to establish eligibility and safety to enter the trial Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial
- Phlebotomy /cannulation training and valid IV drugs/ therapy administration training Monitor treatment toxicity/side effects and initiate changes to treatment or treatment cessation as required by trial protocols Report and record adverse events which occur whilst patients are under trial therapy to the trial co-ordinator/Principal Investigator and relevant local and regulatory authorities Provide continuity of care to participants and their carers throughout the trial programme. Provide specific advice and psychological support as appropriate. Refer to other specialists as required to ensure optimum participants care. Act as a primary contact point for the trial participant Maintain accurate participants trial documentation, complete Case Report Forms, including the use of electronic data capture systems and ensure relevant information is recorded in participants case notes
Job description
Job responsibilities
- Experience required Minimum 2 years post qualification experience Working in the NHS Research experience desirableSuitable for someone who is: Self-motivated, flexible and able to adapt to changing demands, able to process information and interpret accordingly, able to organise own workload and prioritise work as it comes into the department, able to remain calm and professional under pressure and able to respect confidentiality guidelinesKey ResponsibilitiesClinical Work autonomously and assist in the management of a caseload of clinical trial participants whilst working as part of a multi-disciplinary team. Maintain effective communication with people who use our services, carers and professionals to ensure high quality service delivery Identify suitable people who use our services for entry into clinical trials Maintain accurate documentation of participants events in progress notes Ensure people who use our services are fully informed prior to entry into clinical trial programmes Provide ongoing information, education and support to participants (and their significant others) regarding clinical trials and specific trial treatments Ensure that trial specific investigations are undertaken as required by the trial protocol and obtain results in order to establish eligibility and safety to enter the trial Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial
- Phlebotomy /cannulation training and valid IV drugs/ therapy administration training Monitor treatment toxicity/side effects and initiate changes to treatment or treatment cessation as required by trial protocols Report and record adverse events which occur whilst patients are under trial therapy to the trial co-ordinator/Principal Investigator and relevant local and regulatory authorities Provide continuity of care to participants and their carers throughout the trial programme. Provide specific advice and psychological support as appropriate. Refer to other specialists as required to ensure optimum participants care. Act as a primary contact point for the trial participant Maintain accurate participants trial documentation, complete Case Report Forms, including the use of electronic data capture systems and ensure relevant information is recorded in participants case notes
Person Specification
esential
Essential
Desirable
esential
Essential
Desirable
desirable
Desirable
- Previous research experience
Person Specification
esential
Essential
Desirable
esential
Essential
Desirable
desirable
Desirable
- Previous research experience
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.
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.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
