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Research Nurse Bank (Part time, Study Specific) - Clinical Trials, London
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Client:
hVIVO
Location:
London, United Kingdom
Job Category:
Other
-
EU work permit required:
Yes
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Job Reference:
3859109fcfb3
Job Views:
4
Posted:
22.06.2025
Expiry Date:
06.08.2025
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Job Description:
Overview
This is an exciting opportunity for a
part time bank unblinded Research Nurse
to join our team at our FluCamp site in London, E1. As a Research Nurse you will support the Clinical Trial Centre with, day to day planning and execution of a clinical study screening.
hVIVO conducts human challenge studies offering services to both pharmaceutical and biotechnology companies using a range of different clinical trial methodologies across differing viral challenges. The end goal of our clinical trials is to potentially eradicate common illnesses like the common cold and flu completely – or at least make treatment of them as easy and effective as possible. Volunteers are central to the work that we do. Our studies focus on testing new treatments on real people, in a safe, controlled, clinical environment.
The Research Nurse plays a key role in the provision of nursing support and duties for optimal study delivery from clinical start-up to clinical close out as either an individual contributor, performing study coordinator duties on trials, or as a line manager to the support roles.
This role is to work on a specific trial covering particular duties. Working on shifts Monday to Sunday
08:00 – 1400.
Starting date of either 15th January or 22nd January, you will be required to complete three days of training plus a shadow shift.
(Note the above hours may vary slightly as study is in planning stages and this will be determined closer to the time).
Additonal hours may be available beyond the contract if there is an operational need.
Please note, hVIVO works with a range of respiratory viruses as part of our day to day operation. It is recommended you consider your own health and those of family members when considering to apply for this role.
Main Responsibilities
This role covers specific duties from a range of the below responsibilities.
Administer IMP to volunteers
To maintain and promote the safety and wellbeing of all subjects participating in a clinical trial within the regulatory frameworks of ICH GCP, other statutory instruments and NMC Code of Conduct.
Assist the senior team with the daily management and allocation of workload within the clinical environment
Involvement in preparing, planning and execution of daily clinical activities;
Provide guidance and mentoring to staff in the clinical environment. Ensure competence in performing their own and team’s daily tasks;
Supervision of new ancillary staff in the clinical environment as required;
Promote and adhere to Company SOP’s, protocols and Health and Safety Regulations; and
Support Clinical Support Specialists in performing clinical assessments as per protocol;
Perform nurse specific procedures as identified within the protocol;
Performs informed consent procedures as identified in the study protocol;
Completion of study related documents e.g. logs, source data and CRFs;
Adhere to Company SOPs, protocols and Health and Safety Regulations;
Use of expertise to input into the development of SOPS and other procedural documents;
Maintain subject safety at all times responding to emergencies as per internal SOP and national guidelines and protocols;
Monitoring and identification of the deteriorating subject, with appropriate escalation;
Responsible for the checking of emergency resuscitation equipment as per SOP/OIs;
Responsible for maintenance of medicines management within the clinical department as per SOP/OI;
Responsibility for the supervision of clinical staff in the screening unit as delegated by the Senior Research Nurse;
Identification of areas for service improvement;
Promotes a high standard of practice and care at all times
Skills & Experiences
IMP dosing experience in research essential
Knowledge of GCP and previous experience in a clinical trials setting essential
Completed Immunisation and Vaccination (DPC Healthcare providers)
Certificate in basic or intermediate life support essential
Sound clinical knowledge
Competence in the recording of medical history, vital signs, ECG, phlebotomy etc essential
Ability to work within the Team
Effective organisational skills
Ability to work with a degree of flexibility
Ability to prioritise own workload
Competence in the recording of: medical history, vital signs, ECG, phlebotomy and the ability and willingness to learn new skills
Ability to manage adverse events or clinical incidents
An understanding of ethical practice and confidentiality
Good IT skills including Word and Excel
Strong and demonstrated attention to detail
Good knowledge of ICH-GCP and regulatory standards
Willingness to learn additional skills
Ability to work independently and within the team
Positive and Supportive Team player
Options
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Overview
This is an exciting opportunity for a
part time bank unblinded Research Nurse
to join our team at our FluCamp site in London, E1. As a Research Nurse you will support the Clinical Trial Centre with, day to day planning and execution of a clinical study screening.
hVIVO conducts human challenge studies offering services to both pharmaceutical and biotechnology companies using a range of different clinical trial methodologies across differing viral challenges. The end goal of our clinical trials is to potentially eradicate common illnesses like the common cold and flu completely – or at least make treatment of them as easy and effective as possible. Volunteers are central to the work that we do. Our studies focus on testing new treatments on real people, in a safe, controlled, clinical environment.
The Research Nurse plays a key role in the provision of nursing support and duties for optimal study delivery from clinical start-up to clinical close out as either an individual contributor, performing study coordinator duties on trials, or as a line manager to the support roles.
This role is to work on a specific trial covering particular duties. Working on shifts Monday to Sunday
08:00 – 1400.
Starting date of either 15th January or 22nd January, you will be required to complete three days of training plus a shadow shift.
(Note the above hours may vary slightly as study is in planning stages and this will be determined closer to the time).
Additonal hours may be available beyond the contract if there is an operational need.
Please note, hVIVO works with a range of respiratory viruses as part of our day to day operation. It is recommended you consider your own health and those of family members when considering to apply for this role.
Main Responsibilities
This role covers specific duties from a range of the below responsibilities.
Administer IMP to volunteers
To maintain and promote the safety and wellbeing of all subjects participating in a clinical trial within the regulatory frameworks of ICH GCP, other statutory instruments and NMC Code of Conduct.
Assist the senior team with the daily management and allocation of workload within the clinical environment
Involvement in preparing, planning and execution of daily clinical activities;
Provide guidance and mentoring to staff in the clinical environment. Ensure competence in performing their own and team’s daily tasks;
Supervision of new ancillary staff in the clinical environment as required;
Promote and adhere to Company SOP’s, protocols and Health and Safety Regulations; and
Support Clinical Support Specialists in performing clinical assessments as per protocol;
Perform nurse specific procedures as identified within the protocol;
Performs informed consent procedures as identified in the study protocol;
Completion of study related documents e.g. logs, source data and CRFs;
Adhere to Company SOPs, protocols and Health and Safety Regulations;
Use of expertise to input into the development of SOPS and other procedural documents;
Maintain subject safety at all times responding to emergencies as per internal SOP and national guidelines and protocols;
Monitoring and identification of the deteriorating subject, with appropriate escalation;
Responsible for the checking of emergency resuscitation equipment as per SOP/OIs;
Responsible for maintenance of medicines management within the clinical department as per SOP/OI;
Responsibility for the supervision of clinical staff in the screening unit as delegated by the Senior Research Nurse;
Identification of areas for service improvement;
Promotes a high standard of practice and care at all times
Skills & Experiences
IMP dosing experience in research essential
Knowledge of GCP and previous experience in a clinical trials setting essential
Nursing qualification essential
NMC registration essential
Completed Immunisation and Vaccination (DPC Healthcare providers)
Certificate in basic or intermediate life support essential
Sound clinical knowledge
Competence in the recording of medical history, vital signs, ECG, phlebotomy etc essential
Good patient communication skills essential
Ability to work within the Team
Good time management skills
Effective organisational skills
Ability to work with a degree of flexibility
Ability to prioritise own workload
Competence in the recording of: medical history, vital signs, ECG, phlebotomy and the ability and willingness to learn new skills
Ability to manage adverse events or clinical incidents
An understanding of ethical practice and confidentiality
Good IT skills including Word and Excel
Strong and demonstrated attention to detail
Good knowledge of ICH-GCP and regulatory standards
Willingness to learn additional skills
Ability to work independently and within the team
Positive and Supportive Team player
Options
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