Job summary
The job is fixed term for 12 months with further scope of extension. The post holder will support and manage high quality clinical research in Oncology, according to ICH good clinical practice guidelines. The post holder will work closely with Dr Tom Newsom-Davis, other oncology consultants, and oncology Clinical Investigators. The CRF will be involved in the delivery of clinical trials and the development of trial protocol and clinical guidelines. The post holder will ensure that governance arrangements are maintained throughout duration of studies and that studies are managed in accordance with study protocols, national and international legislation and guidance (e.g. UK Policy Framework for Health and Social Care, Clinical Trial Regulations, GCP). They will also assess patient suitability for studies, screening, obtaining informed consent, recruiting patients in line with agreed targets, data collection and maintaining research study records. The CRF are also expected to ensure that all research safeguards the psychological and physical well-being of the patient in conjunction with medical and nursing staff to facilitate high standards of care with regards to research. The CRF is expected work across the Trust, attend local and national meetings, present at conferences, write up and publish their work in medical indexed journals.
Main duties of the job
Research Responsibilities
a) To contribute to study protocol design in collaboration with Clinical Research Lead and Pharmaceutical Companies and Academic Institutions representatives. This may include the writing of participant information leaflets, design of case report forms and source documents in line with the R&D standard operation procedures (SOPs).
b) To write concept sheets and full protocols or amend such documents which relate to the primary research carried out in Oncology.
c) Contribute to the promotion of Chelsea and Westminster Hospital Research and Development and creating further funding opportunities.
d) To represent the unit at meetings both locally and as required, at national and international locations; this includes Investigator meetings and Study Initiation meetings as well as attendance at Research Ethics Committee meetings.
e) To undertake clinical responsibilities and research activities in Phase I-IV Research in Oncology.
f) To provide clinical and professional supervision in collaboration with Assistant Director Research and Development to doctors and other staff (e.g. research nurses, research assistants etc.).
g) To ensure that the dignity, right, safety, and wellbeing of all trail participants and give priority at all times
About us
Chelsea and Westminster Hospital NHS Foundation Trust is one of England's top-performing and safest trusts. We operate two main acute hospital sites--Chelsea and Westminster Hospital and West Middlesex University Hospital--along with award-winning clinics across North West London.
Our nearly 7,500 staff care for a diverse population of 1.5 million, providing full clinical services, including maternity, A&E, and children's services, plus specialist HIV and sexual health clinics. The Care Quality Commission rates us 'Good' in safety, effectiveness, care, and responsiveness, and 'Outstanding' in leadership and resource use.
We continually invest in our facilities, including a £30m expansion of critical care at Chelsea and Westminster and an £80m Ambulatory Diagnostic Centre at West Middlesex.
We are committed to equal opportunities and believe that diversity drives innovation and excellence. As part of our dedication to equity, we actively welcome applications from individuals from the global majority, veterans and underrepresented communities. We value the unique perspectives and experiences that diverse teams bring and are committed to creating an environment where all voices are heard, respected, and empowered to succeed."
If you haven't heard from us within three weeks of the closing date, your application was likely unsuccessful. Employment is subject to a six-month probationary period.
Some roles may require weekend shifts at multiple sites.
Job description
Job responsibilities
Roles and responsibilities Item 1
Other Research Responsibilities:
To keep well organised, legible and accurate records.
To meet with study monitors regularly to assist with clarification of data queries in order to maintain quality assurance
To participate in audits or inspection of Trust sponsored clinical trials as well as external sponsored studies as required.
To assist in both internal and external training requirements (general and study-specific) in liaison with Lead Nurse and other Clinicians.
The post-holder will be required to build on existing close relations with colleagues as part of a multidisciplinary team. They will also be required to support quality improvement, research and management of the service.
Item 2
Other Clinical Responsibilities:
Adhere to the Trust Customer Service Commitment and adopt a professional approach to customer care at all times.
Develop clinical practice through self-reflection and learning from experience, application of research into practice and active contribution within the multi-disciplinary team.
Demonstrate, model and encourage trust values at all times to all patients and staff. Participate in audit and quality improvement
As a Clinical Research Fellow you will be involved in clinical duties, providing clinical care to patients in outpatient Clinics as required by the service.
Item 3
Finance Responsibilities: To actively contribute with the cost calculation of studies in Oncology. Sensible management of studies resources.
Item 4
General Responsibilities
o Pay due regards to your own safety and the safety of others.
o Adhere to protocol laid down, SOP and ICH GCP Guidelines.
o Seek and give advice as appropriate
o Ensure that standard of quality and safety is maintained.
Job description
Job responsibilities
Roles and responsibilities Item 1
Other Research Responsibilities:
To keep well organised, legible and accurate records.
To meet with study monitors regularly to assist with clarification of data queries in order to maintain quality assurance
To participate in audits or inspection of Trust sponsored clinical trials as well as external sponsored studies as required.
To assist in both internal and external training requirements (general and study-specific) in liaison with Lead Nurse and other Clinicians.
The post-holder will be required to build on existing close relations with colleagues as part of a multidisciplinary team. They will also be required to support quality improvement, research and management of the service.
Item 2
Other Clinical Responsibilities:
Adhere to the Trust Customer Service Commitment and adopt a professional approach to customer care at all times.
Develop clinical practice through self-reflection and learning from experience, application of research into practice and active contribution within the multi-disciplinary team.
Demonstrate, model and encourage trust values at all times to all patients and staff. Participate in audit and quality improvement
As a Clinical Research Fellow you will be involved in clinical duties, providing clinical care to patients in outpatient Clinics as required by the service.
Item 3
Finance Responsibilities: To actively contribute with the cost calculation of studies in Oncology. Sensible management of studies resources.
Item 4
General Responsibilities
o Pay due regards to your own safety and the safety of others.
o Adhere to protocol laid down, SOP and ICH GCP Guidelines.
o Seek and give advice as appropriate
o Ensure that standard of quality and safety is maintained.
Person Specification
Experience of audit, quality improvement and Research
Essential
- Experience of setting up and conducting clinical research. Oncology Clinical experience
Desirable
- Clinical and educational supervision experience
- Special interest in medical or clinical oncology
- Sold understanding of Good Clinical Practice
Person Specification
Experience of audit, quality improvement and Research
Essential
- Experience of setting up and conducting clinical research. Oncology Clinical experience
Desirable
- Clinical and educational supervision experience
- Special interest in medical or clinical oncology
- Sold understanding of Good Clinical Practice
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).
Employer details
Employer name
Chelsea and Westminster Hospital NHS Foundation Trust
Address
Chelsea and Westminster and West Middlesex Hospital sites
369 Fulham Rd
London
SW10 9NH
Employer's website
https://www.chelwest.nhs.uk/ (Opens in a new tab)