hVIVO are currently seeking an addition to our Data Entry team to work across our London sites in Whitechapel & Canary Wharf, East London.   hVIVO conducts 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. 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 Data Entry team ensure accurate entry of study data into data management systems and provide administrative assistance to the Data Associate/Project Data Manager on assigned studies.   This is for a zero hours contract initially and the pay rate is £12/hour. The successful candidate can expect to work full time hours and a good full time availability is required.

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 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.

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 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 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 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 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.