Job summary
The Royal Marsden NHS Foundation Trust is one of the world's leading cancer research centres. The Trust works in partnership with The Institute of Cancer Research to produce high quality basic research, translational studies and clinical trials with the aim of developing better treatments for the benefit of cancer patients worldwide.An opportunity has arisen to work within the Haemato-Oncology Unit as a Research Nurse providing support for our complex research portfolio during a 12 month maternity cover.This is a pivotal role and you will be part of a multidisciplinary team including experienced medical and research staff, taking part in an exciting range of clinical research studies. Ideally with previous clinical research experience, you will work within the guidelines and policies for the conduct of clinical trials, ensuring high standards of practice in accordance with the principles of GCP.The successful applicant will be required to work as a self directed practitioner and have the skills to motivate others. They should also have a flexible approach to their duties and the ability to work both as part of the team as well as independently. In addition, you will have excellent communication, administrative and IT skills and be supportive and open to new initiatives.
Main duties of the job
The post holder will work under the supervision of the lead/senior research nurse or Study Site Coordinators (SSC) within the Haemato-Oncology research team and has a key role to play in the dayto- day running of clinical trials within the Trust. These trials may be related to anti-cancer treatment
(e.g. chemotherapy, radiotherapy, biological therapy, gene therapy or surgery), symptom management or some other aspect of cancer care, such as screening. Central to the role are the recruitment, education and monitoring of patients entering a clinical trial. Working closely with the principal investigator and members of the multidisciplinary team, s/he will support patients who choose to participate in clinical trials by providing advice and information and acting as the patients' advocate. An important aspect of the role is the maintenance of accurate and comprehensive records of data derived from the research studies.
The post holder will support more junior research nurses, assisting them to develop their clinical research skills thorough education and training. Further responsibility will include monitoring and raising the standard of nursing input within the team.
The opportunity to undertake personal research projects or further study, in consultation with the lead medical investigator and Lead Nurse Clinical Trials, is also encouraged.
About us
The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals - one in Chelsea, London, and one in Sutton, Surrey - as well as a Medical Daycare Unit in Kingston Hospital
At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.
At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits and learning and development opportunities. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.
Job description
Job responsibilities
For further information on this role, please see the attached detailed Job Description and Person Specification
To co-ordinate arrangements required for patients undergoing specialist investigations as part of the research protocol.
To assess the patient prior to trial treatment, monitor the patient receiving trial treatment and follow the patient up on completion of trial treatment as required by the protocol.
To collect and accurately record data in accordance with the requirements of the trial protocol.
To participate in the design and preparation of research protocols, patient information sheets and other documentation associated with clinical trials, ensuring that these are reviewed and updated as required.
To safeguard the integrity of the trial by ensuring compliance with ICH GCP guidelines
To provide advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent, ensuring the patient (or where appropriate the parent/ guardian or next of kin) fully understands the nature of the clinical trial, of voluntary entry to the clinical trial and freedom to withdraw at any time without prejudice to treatment.
To act as a support for patients and relatives throughout the trial, providing information as well as physical, spiritual and emotional support where necessary, and referring to other healthcare professionals where appropriate.
Job description
Job responsibilities
For further information on this role, please see the attached detailed Job Description and Person Specification
To co-ordinate arrangements required for patients undergoing specialist investigations as part of the research protocol.
To assess the patient prior to trial treatment, monitor the patient receiving trial treatment and follow the patient up on completion of trial treatment as required by the protocol.
To collect and accurately record data in accordance with the requirements of the trial protocol.
To participate in the design and preparation of research protocols, patient information sheets and other documentation associated with clinical trials, ensuring that these are reviewed and updated as required.
To safeguard the integrity of the trial by ensuring compliance with ICH GCP guidelines
To provide advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent, ensuring the patient (or where appropriate the parent/ guardian or next of kin) fully understands the nature of the clinical trial, of voluntary entry to the clinical trial and freedom to withdraw at any time without prejudice to treatment.
To act as a support for patients and relatives throughout the trial, providing information as well as physical, spiritual and emotional support where necessary, and referring to other healthcare professionals where appropriate.
Person Specification
Education/Qualifications
Essential
- NMC registration
- Post registration experience in a cancer care / acute care environment
- BSc/MSc or studying at relevant level
- Evidence of Continuing Professional Development
Desirable
- Recognized cancer nursing qualification
- Research methods education
Experience
Essential
- Experience as a research nurse/senior staff nurse working in a clinical research environment
- Experience as a research nurse/senior staff nurse in oncology nursing
Desirable
- Previous experience in clinical specialty of haematology
- Personal and leadership management experience
Skills/Abilities/Knowledge
Essential
- Excellent organisational and time management skills
- Excellent cross-disciplinary communication skills and ability to facilitate collaborative working relationships
- Able to work unsupervised
- Ability to work under pressure in order to meet service and patient priories
- Computer literate in Microsoft outlook, office, word, excel and PowerPoint
Person Specification
Education/Qualifications
Essential
- NMC registration
- Post registration experience in a cancer care / acute care environment
- BSc/MSc or studying at relevant level
- Evidence of Continuing Professional Development
Desirable
- Recognized cancer nursing qualification
- Research methods education
Experience
Essential
- Experience as a research nurse/senior staff nurse working in a clinical research environment
- Experience as a research nurse/senior staff nurse in oncology nursing
Desirable
- Previous experience in clinical specialty of haematology
- Personal and leadership management experience
Skills/Abilities/Knowledge
Essential
- Excellent organisational and time management skills
- Excellent cross-disciplinary communication skills and ability to facilitate collaborative working relationships
- Able to work unsupervised
- Ability to work under pressure in order to meet service and patient priories
- Computer literate in Microsoft outlook, office, word, excel and PowerPoint
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).
