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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 0700 - 1200 and 1900 - 0000. These hours may vary once the trial is underway.
Starting date in April, you will be required to complete three days of training (Monday to Friday) plus two shadow shifts (including Saturday and Sunday).
(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.
hVIVO are currently looking for an Associate Project Manager to join the Project Management team. This role is working at home as well at our offices in London E1 and E14 (from mid 2024).
Please note this is a 12 month fixed term contract to cover maternity leave and is to start as soon as possible.
hVIVO conducts human challenge clinical trials. 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 Associate Project Manager is responsible, under direction of a Project Lead, for supporting the delivery of the project to timelines, within budget and to agreed quality standards working closely with their allocated cross-functional team.
hVIVO is currently seeking a motivated, versatile and forward thinking Pharmacy Assistant to join the FluCamp team to work accross our sites in Whitechapel & Canary Wharf.
hVIVO conducts human challenge clinical trials. 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
You will work in a team of Pharmacy Assistants and our Pharmacist, to cover shifts in our clinical trials units participating in the preparation, return and dispensing of investigational products for Clinical Trial participants.
Our sites require cover across a variety of shifts Monday-Sunday, day and night shifts. Shifts in the unit include the following:
- 0500-1300
- 0900-1700
- 1500-2300
You will be expected to commit to at least one shift a week and we can offer a maximum of three shifts currently. You will also be required to commit to a two week, full-time training period.
hVIVO is a dynamic and pioneering global player in the pharmaceutical early phase research sector, and has been recently developing a strong discovery (research and development) focus to investigate human disease to help find better treatments, faster. We are always interested to hear from similarly dynamic and pioneering individuals who share our vision to better understand the more precise nature of human disease and to really make a difference.
As a both an office- and laboratory-based role, the Senior Development Scientist is responsible, as a scientific lead and expert, for the management and conduct of internal and external studies, either as part of hLab only business or in the development and validation of new methodologies and reagents for subsequent utilisation in hLab. The Senior Development Scientist will provide Scientific Operational support for hLab and will also provide scientific mentorship and scientific staff development of other hLab junior staff as well as conducting study plans, report reviews and data analysis.
hVIVO are seeking a Research Assistant to join the Development Team at our site in London, E1. The Research Assistant (RA) will be responsible for the support of internal and external studies and in the development and validation of new methodologies and reagents for subsequent utilisation.
The Development team are responsible for the development and validation of molecular, virology and immunology assays in line with hVIVO corporate objectives and priorities.
hVIVO is a dynamic and pioneering global player in the pharmaceutical early phase research sector, and has been recently developing a strong discovery (research and development) focus to investigate human disease to help find better treatments, faster. We are always interested to hear from similarly dynamic and pioneering individuals who share our vision to better understand the more precise nature of human disease and to really make a difference.
hVIVO are currently seeking a BioBank Assistant to join the Laboratory Operations team at our site in Ely.
The main focus of the BioBank Assistant role is performing receipt & storage of clinical trial participant samples in accordance with GCP, HTA, IATA and ADR. They also provide technical support to the wider team at hVIVO to ensure safe storage, handling, and transport of samples with a prime focus on quality.
hVIVO conducts human challenge clinical trials. 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. clinical trial participants are central to the work that we do. Our studies focus on testing new treatments on humans, in a safe, controlled, clinical environment.
We currently require a commitment to full-time hours working 37.5 hours a week, with potential paid, on-call, out of hours responsibilities.
The pay rate is curently £11/hour. You would be employed via a third party agency and pad weekly.
This is an exciting opportunity for a Research Nurse to join hVIVO to support the daily planning and execution in our clinical study screening department in E1 and E14 (mid 2024).
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 cost-effective 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.
The shift patterns for this role are as follows, with the roster provided a month prior.
0730 - 1530 AM shift
1230 - 2030 PM shift
1930 - 0830 Night shift (approx 3 per month)
hVIVO is currently seeking a motivated, versatile and forward thinking Pharmacist to join the FluCamp team accross our sites in London E1 & E14 to start as soon as possible.
hVIVO conducts human challenge clinical trials. 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 Pharmacist will lead on all aspects of IMP Management, including planning, accountability, formulation and destruction according to study protocols and will be primary contact for all IMP related activities, documentation, client and vendor management.
Working hours for this role are 37.5 hours per week ranging from 5am starts to 11pm finish.
hVIVO is a dynamic and pioneering global player in the pharmaceutical early phase research sector. We conduct human challenge studies offering services to both pharmaceutical and biotechnology companies using a range of different clinical trial methodologies. 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. Our studies focus on testing new treatments on real people, in a safe, controlled, clinical environment.
This is an exciting time of growth for the company and we are looking to strengthen the Business Development Team with a Business Development Director, to help focused on the sales of clinical site services
This is an exciting opportunity for a Senior Research Nurse to join our team at hVIVO working in the pioneering world of human based clinical trials. This is a full-time, permanent role based between Whitechapel, E1 and Canary Wharf, E14 (from mid 2024).
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 Senior Research Nurse plays a key role in the coordination of clinical unit activities, appropriate staff scheduling , the development of quality service delivery, providing management, support and guidance to all staff and ensuring a GCP customer focussed service from screening to final study visit.
Practicing at an advanced level demonstrating a high level of autonomy and clinical decision-making, performing diverse responsibilities requiring considerable analysis, judgment, and detailed understanding of clinical research processes and staff development and engagement.
Acting as clinical project lead from clinical start-up to close out, this role is responsible for providing support as study coordinator on trials, and as a line manager for Research Nurses. This role provides mentoring and supervisory support to the clinical team, study support to project teams and to maintain a ward environment conducive to study delivery. With other members of the senior clinical team, the Senior Research Nurse ensures that all staff work in accordance to evidence based nursing practice, maintaining high standards of care.
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 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.
hVIVO are seeking a Laboratory Technician to join the Laboratory team accross our sites in London, E1 & E14.
The Laboratory Technician performs processing, storage and transport of subject’s samples according to Good Clinical Practice (GCP) standards and provides technical support to the wider team at hVIVO sites to ensure effective laboratory operation with a prime focus on quality in everything they do.
hVIVO conducts human challenge clinical trials. 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 offer is for casual hours on zero hours contract via a third party agency. The pay rate is £11/hour. You will need a flexible availability for shifts Monday - Sunday.
hVIVO is a world leader in human challenge clinical trials. 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
We are expanding our operations and part of this expansion, we are investing in our next generation systems. To support this, we are looking for an IT Application Specialist, a crucial role in developing and maintaining our strategic systems based on Salesforce and Veeva platforms.
Exciting times to join the team, with offices based in our office in E1 (Whitechapel/Aldgate East)
hVIVO are currently looking for a proactive and experienced Research Scientist (RS) to join our laboratory team across our sites in E1 & E14. The RS position is a key role within lab operations and is critical in assisting in the delivery of clinical trials.
The hVIVO Laboratory function undertakes the sample processing and analysis for all clinical trials conducted at hVIVO. The RS position exposes applicants to a range of practical techniques including Qualitative and Quantitative PCR, cell infectivity, neutralising antibody, serology assays and multiplex viral detection assays. The laboratory division has a diverse work stream including internal studies, clinical trials and standalone projects. The laboratory division also performs bespoke assay development and validation work and collaborates with strategic partners.
The RS will work as part of our Laboratory Operations Department supporting the delivery of clinical trials. The wider team includes individuals with a wide range of experience including Research Assistants, specialists in specific areas and Senior Virologists.
The RS role is a lab focused position with room to develop and refine practical laboratory skills. The day to day work includes processing samples, performing assays and analysing data. The role offers significant growth as the position also requires leading projects (internal and external) by acting as Study Lead (SL). The SL is responsible for the smooth day to day running of the analytical phase of clinical trials performed at hVIVO, working under the guidance of a senior scientist. This gives applicants exposure to the responsibility and skills required for future project management positions. The SL role includes study resource management, matrix management of colleagues, and responsibility for data review and quality, sample logistics, document writing and delivery of training.
The role involves working to a flexible shift pattern including working evenings and weekend as required to deliver the operational plan.
The ideal candidate will have a virology/biomedical background, and have experience working to GCP / GLP as part of a CRO or pharmaceutical company. They will be degree educated or above and have hands-on experience of key virology techniques including tissue culture, cell-based infectivity assays and qPCR. They will be a proactive individual with a desire to learn and progress in a GCP environment. The candidate will be flexible with working patterns to suit the needs of the business.
hVIVO are seeking a Principal Scientisit ( Immunology or Virology ) to act as our SME providing consultative advice across multiple projects and throughout the business.
hVIVO conducts human challenge clinical trials. 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 Principal Scientist will take a lead role in the scientific development of all lab operational staff. Working with line managers develop training plans and material and deliver study lead / study management training program.
This is a client facing role, involving detailed scientific discussions to support clients in the setup of their projects. That include needing a detailed technical understanding of all lab assays and processes, as well as detailed understanding of the fields of virology or immunology.
In addition, this role is responsible for analysing and reporting scientific and strategic risks and options and making their recommendations to senior management.
hVIVO are currently looking for a Research Assistant (RA) to join our laboratory team at our site in east London. The RA role is a key role within lab operations assisting in the delivery of clinical trials processing samples, performing assays and data analysis.
The hVIVO Lab function supports the delivery of clinical trials for external and internal clients by performing sample processing and analytical techniques including Qualitative and Quantitative PCR, cell infectivity, neutralising antibody and serology assays, and multiplex viral detection assays. This is done for clinical trials performed at hVIVO and for external trials. The Lab also perform bespoke assay development and validation work and collaborates with strategic partners.
The role involves working to a flexible shift pattern including working evenings and weekend as required to deliver the operational plan.
The ideal candidate will have a virology/ biomedical background working to Good Clinical Practice (GCP) as part of a Clinical Research Organisation (CRO) or pharmaceutical company. They will be degree educated and have hands on experiences of key virology techniques including tissue culture, cell based infectivity assays and qPCR. Be a proactive individual with a desire to learn and progress in a GCP environment. Be flexible with working patterns to suit the needs of the business.
hVIVO are seeking a Development Scientist to join our team of scientists who are responsible for the development and validation of molecular, virology, microbiology and immunology assays in line with hVIVO corporate objectives and priorities. The Development Scientist will also lead bespoke R&D client projects as part of lab services and contribute to the business and lab capabilities development strategy, engaging directly with clients as required.
hVIVO is a dynamic and pioneering global player in the pharmaceutical early phase research sector, and has been recently developing a strong discovery (research and development) focus to investigate human disease to help find better treatments, faster. We are always interested to hear from similarly dynamic and pioneering individuals who share our vision to better understand the more precise nature of human disease and to really make a difference.
The candidate should have proven experience of being able to prioritise and deliver multiple activities in-line with the agreed strategy and be able to effectively communicate progress and risks to management. They should be able to demonstrate the ability to work independently, managing time efficiently and analysing complex data sets to compile into presentable formats. They should have experience of training and mentoring junior staff as well as the management of the operational delivery of their projects. They should have strong communication skills, keeping management informed of progress in project delivery. Experience in oral presentations and written outputs would be an advantage. They should have a good understanding of and worked in an environment governed by a quality management system (GCP, GLP, ISO, GMP). Specific experience of working to regulatory guidelines in compliance with Good Clinical Practice and Good Clinical Practice for Laboratories would be an advantage.