hVIVO are currently looking for a Laboratory Assistant to join our laboratory team at our site in Whitechapel E1.    hVIVO conducts human challenge studies offering services to both pharmaceutical and biotechnology companies using a range of different 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. Our studies focus on testing new treatments on real people, in a safe, controlled, clinical environment.   The Laboratory Assistant will provide the required technical support to enable the laboratory team to function effectively whilst adhering to GCP, SOP’s and health and safety guidelines.   They will assist in the maintenance of the lab, cleaning of equipment, reagent/chemical delivery tasks and preparation of smple kits.   Working hours are 5 hours per day, 0900-1400, Monday-Friday on £11/hour. You will be employed via a third party agency and not diretcly with hVIVO.

hVIVO is currently seeking a motivated, versatile and forward thinking Pharmacy Assistant to join the FluCamp team in London E1 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   You will work in a team of Pharmacy Assistants to cover shifts in our clinical trials unit participating in the preparation, return and dispensing of investigational products for Clinical Trial participants. Y   We are currently seeking 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

hVIVO are seeking a Systems Analyst to join the IT team at our main site in London, E1 on a fixed term contract for 12 months.   The Systems Analyst will support the improvement of systems for end users within the business.   The role will be accountable for gathering user requirements from different operational areas of the business. Document and test against these requirements in line with regulatory requirements. You will be responsible for ensuring the look, feel, and functionality of our websites, apps, and web applications meet user needs.   You will work closely with external partners to deliver on key system projects and use your industry knowledge to drive efficiencies while providing a single voice for business requirements.   Duties will be split between project work and day to day support, and general IT support for end users.  

hVIVO is recruiting for an experienced Quality Assurance Auditor. This is a permanent position based in London (E1) and is site based approximately 3 days per week.   The main purpose of the role is to ensure that hVIVO are in compliance with the relevant SOPs, regulations and internationally recognised guidelines (including Statutory Instrument 2004 No. 1031 and its amendments, ICH GCP and GCP for laboratories). It is also to Conduct audits of all systems, processes, facilities, documents and studies within hVIVO and of suppliers and subcontractors to hVIVO in order to deliver the audit programme as required by GCP.   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.

hVIVO is an exciting and rapidly growing specialist contract research organisation (CRO) and the world leader in testing infectious and respiratory disease vaccines and antivirals using human challenge trials. We provide end-to-end early clinical development services for our broad and long-standing client base of global biopharma companies. The Assistant Financial Accountant will be a key member of the Finance team, responsible for assisting the Group Financial Controller in delivering accurate, compliant and timely Financial Statements, Tax returns, cash flow, receivables and month end reporting. As part of the monthly and yearly reporting cycles, duties will include certain balance sheet reconciliations, billing and accounts receivable support, preparation of VAT and other tax returns, payroll support and the monitoring of timesheets to support the Group’s revenue recognition.  

This is an exciting opportunity for a part time 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. There are two specific shift patterns Monday to Sunday for a three (3) month period starting from early July. You would not be required to work both shifts in the same day.   AM Shift – 08:00/09:00 – 12:00/13:00 PM Shift – 20:00/21:00 – 00:00/01:00   (Note the above hours have an hours' variation as this will be determined closer to the time). There is transport support for those working on the PM shift.    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 Cinical Trial Administrator to administer, maintain and co‑ordinate the logistical aspects of all hVIVO projects and act as a pivotal point of contact for the project teams and any vendor and affiliate organisations. they will assist Project Managers/Directors in co-ordinating and conducting clinical studies and trials in a manner that ensures quality, consistency, timeliness, accuracy and patient safety.   hVIVO conducts human challenge studies offering services to both pharmaceutical and biotechnology companies using a range of different clinical trial methods. 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 Clinical Trial Administrator reports to a Project Director, Project Management and works closely with the all members of the project team.   The role will be based in our London offices (E1).

hVIVO is a leading Clinical Research organistion driving innovation in this exciting field. hVIVO are looking for an experienced GxP computer systems validation expert to join our IT department to work on major system implementations for LIMS and clinical E-source systems.  As well as to manage and maintain our company CSV process and champion CSV within the business.      The ideal candidate will have around 10 years experience working with IT computer systems in a GxP environment, will have hands on experience with GxP CSV including implementation of LIMS and / or Clinical electronic data capture systems.  Will have IT technical experience including systems development and a working understanding of infrastructure and systems deployment.   Responsibilities include management of GxP systems used in the collection, storage and reporting of clinical data for the systems full life cycle.  Including creation and maintenance of CSV documentation, vendor management and direct involvement in the initial validations and subsequent change controls of new and existing systems.    This will include the User Requirements Specification, Functional specification, validation plan, test plan and user test cases documentation.  The role will also assist with testing and development of new systems, including systems design and development.    You will be part of project teams for major systems implementations working with the IT project manager and IT developers.  Your project role will be to ensure regulatory compliance of the system, creating the validation package inline with company CSV process.    

hVIVO is a leading Clinical Research organistion driving innovation in this exciting field.  hVIVO are looking for an experienced GxP computer systems validation expert to join our IT department to work on major system implementations for LIMS and clinical E-source systems.  As well as to manage and maintain our company CSV process and champion CSV within the business.      The ideal candidate will have around 10 years experience working with IT computer systems in a GxP environment, will have hands on experience with GxP CSV including implementation of LIMS and / or Clinical electronic data capture systems.  Will have IT technical experience including systems development and a working understanding of infrastructure and systems deployment.   Responsibilities include management of GxP systems used in the collection, storage and reporting of clinical data for the systems full life cycle.  Including creation and maintenance of CSV documentation, vendor management and direct involvement in the initial validations and subsequent change controls of new and existing systems.    This will include the User Requirements Specification, Functional specification, validation plan, test plan and user test cases documentation.  The role will also assist with testing and development of new systems, including systems design and development.    You will be part of project teams for major systems implementations working with the IT project manager and IT developers.  Your project role will be to ensure regulatory compliance of the system, creating the validation package inline with company CSV process.    

We are looking for an experienced Quality Operations Specialist to join our QA team here at hVIVO. The role is to be responsible for the management of QMS Documents, provide quality advice and support in relation to Policies, SOPs, and Master Forms as well as the management for eQMS (electronic quality document management system) system.   Additionally, the role is responsible for leading and having oversight of the Management of the Regulatory Archives (Paper and Electronic)across all hVIVO sites to ensure compliance with regulatory standards and guidelines.   

hVIVO are seeking a  IT Systems Engineer to join the IT team at our offices in London, E1 on a permanent basis.   Fantastic opporutnity to help drive innovation within the infrastructure team in this innovative clinical trials organisation, You will work as a key member of the IT team; to support the IT Business Operations and applications across the group.  This includes ownership of the server and cloud estate and responsibility for best practice in the department.   You will be part of a technical team that drives the operations of IT for the business to improve efficiencies; ensuring up-time, maintenance, development and enhancement in a fast moving, dynamic environment.   It is essential to have excellent customer service skills dealing with a cross section of the business at all levels, external partners and suppliers. 

hVIVO is pioneering a human-based clinical trial platform to accelerate drug and vaccine development in respiratory and infectious diseases. Leveraging human disease models in flu, RSV, HRV and respiratory indications, the hVIVO platform captures disease in motion, illuminating the entire disease life cycle from healthy to sick and back to health.  Our vision remains to become the partner of choice for companies developing products in airways disease that are seeking to gain early proof of concept around the effectiveness of their products and identify the ideal patient profile for later stage clinical development.  hVIVO has established itself as the world leader in human challenge models We are currently recruiting for a Screening Study Physician for our team in Manchester. You will provide screening and assessment of subjects throughout their participation in the clinical trial process ensuring all assessments and procedures are carried out and documented within the protocol requirements/SOP/OIs and according to ICH GCP, other statutory instruments and GMC requirements. Please note, hVIVO works with a range of respiratory viruses as part of our day to day operation, including Covid-19. Your suitability will be part of the interview process from a health and safety perspective and it is recommended you consider your own health and those of family members (clinically vulnerable and shielding) when considering to apply for this role.  

hVIVO are currently seeking a Trainee Internal GCP Auditor to work from our main offices in London, E1.   The Trainee Internal GCP Auditor will conduct audits of company processes, systems, facilities, studies and documents including computer system validation documents to ensure compliance throughout the company.   They will provide flexible administrative support to the QA Department in order to ensure GCP compliance. Support with CAPA investigations, eQMS (electronic quality document management system) and archiving activities as required.

Venn Life Sciences (part of the hVIVO Group) is an Integrated Drug Development partner offering a unique combination of drug development consultancy, clinical trial design expertise and biometry activities. Venn’s capabilities and expertise include: CMC, Non-Clinical, Clinical Development, Biometry and Regulatory Affairs. We have dedicated operations in France, the Netherlands and the UK.   Venn Life Sciences biometry Services offers a unique set of high quality, innovative data management and biostatistics services utilizing new technologies and expertise to help our Sponsors have access to their data faster and at a lower cost.  We work in partnership with our customers to scientifically contribute to the clinical development plans.   We are currently seeking a Senior Biostatistician to join our team. Biostatistics activities are based in Paris, France. Ideally the position will be part-time office-based in the Paris office, part-time homebased. The position will report to the Head of Biostatistics.

FluCamp are looking for two part time (10 to 15 hours pw) Brand Embassador's (can be student working around studying) to support and connect with our volunteer audience as part of our FluCamp (Clinical Trials) brand. One will be London based and one Manchester based.   We conducts human challenge clinical trials. The end goal of our work 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 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 be able to travel to our respective screening facilities in London (E1) and Manchester (City Centre) to seek guidance and support from the team.   You will be paid £10ph on a casual basis and the spread of hours can be agreed upon. 

We are currently looking for an significantly experienced Senior Research Scientist (SRS) with a Virology, Immunology or Biomedical background with strong project management experience to join our laboratory division.  Experience working to GCP and MHRA standards in a clinical trial environment are also key to this role.     The hVIVO Laboratory function undertakes sample processing and analysis for all clinical trials conducted at hVIVO.  The Laboratory team has a diverse work stream including internal studies, clinical trials and standalone projects.  The laboratory team also performs bespoke assay development and validation work and collaborates with strategic partners. The SRS position requires understanding and experience in a range of practical techniques such as Qualitative and Quantitative PCR, cell infectivity, neutralising antibody, serology assays, and multiplex viral detection assays.    The position has 2 overarching focuses: Leading the analytical stage of clinical trial; and acting as a technical Subject Matter Expert (SME) in the scientific discipline.  The role involves being the laboratory point of contact for clinical trial clients, supervising junior members of staff in a matrix management structure, and taking ownership of study data, making sure it is delivered to GCP standards and within the agreed timelines. The SRS has significant growth opportunities by acting as a SME in their technical area and in project management.   The ability to work independently with minimal supervision is key. Exceptional interpersonal and communication skills are also critical to the role.  The SRS will be expected to not only perform day to day tasks effectively, but also to think strategically when it comes to delivery of their assigned project.   The ideal candidate will have a virology, immunology or biomedical background. They will be experienced in working to GCP as part of a CRO or pharmaceutical company (minimum 6 years’ experience).  They will be degree or PhD educated and have hands on experience of key virology techniques including tissue culture, cell-based infectivity assays and qPCR.  They will have experience working in a matrix management structure leading project teams and delivering quality data in a time pressured environment.  The candidate will be a team player that works well under pressure and can motivate others.  Flexibility with working patterns may be required to suit the needs of the business.    

Venn Life Sciences (part of the hVIVO Group) is a CRO offering a unique combination of drug development consultancy, clinical trial design, data management and statistical expertise. Venn’s capabilities and expertise include: CMC, Non-Clinical, Clinical Development, Biometry and Regulatory Affairs.   We have dedicated operations in France, the Netherlands and the UK.   We are currently seeking a SAS Programmer to join our Data Management team. The position will be based in France (Homebased possible according to profile) and will report to the Head of Data Management.

We are currently looking for an experienced Data Manager  to join our team. The successful candidate will have the opportunity to work from one of our European offices and/or partial home-working.    This role is responsible for data management activities for clinical interventional or non-interventional studies ensuring high quality, timely and cost-effective delivery of the data management elements of projects.   If you are seeking a rewarding and challenging career this could be the perfect opportunity for you.

hVIVO is pioneering a human-based clinical trial platform to accelerate drug and vaccine development in respiratory and infectious diseases. Leveraging human disease models in flu, RSV, HRV and respiratory indications, the hVIVO platform captures disease in motion, illuminating the entire disease life cycle from healthy to sick and back to health.  Our vision remains to become the partner of choice for companies developing products in airways disease that are seeking to gain early proof of concept around the effectiveness of their products and identify the ideal patient profile for later stage clinical development.  hVIVO has established itself as the world leader in human challenge models We are currently recruiting for a Study Physician for our team in London. You will provide screening and assessment of subjects throughout their participation in the clinical trial process ensuring all assessments and procedures are carried out and documented within the protocol requirements/SOP/OIs and according to ICH GCP, other statutory instruments and GMC requirements. Please note, hVIVO works with a range of respiratory viruses as part of our day to day operation, including Covid-19. Your suitability will be part of the interview process from a health and safety perspective and it is recommended you consider your own health and those of family members (clinically vulnerable and shielding) when considering to apply for this role.  

If you have exceptional customer service skills and wish to join a caring, dynamic and committed team, this is a great opportunity to join the FluCamp team as a Volunteer Experience Co-ordinator.     Flucamp (a part of hVIVO), conducts human clinical trials. The end goal of our clinical trials  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 our amazing volunteers, in a safe, controlled, clinical environment.   Volunteers are compensated for their time and you can find more information about the volunteer journey here: https://flucamp.com/everydayhero/   Volunteer Experience Co-ordinators welcome volunteers and confirm their medical history to establish their eligibility for one of our trials. If successful, the volunteers are booked in to attend an initial screening appointment and you will guide them through their journey and answer any questions they may have. Our volunteers are VIP’S, and we aim to provide the highest level of volunteer care, that’s where you come in……   What we offer : - Full training - All equipment provided - Remote working - We can currently offer full and part time positions ranging from 30-37.5 hour accross Monday-Sunday New starters can expect a full training programme and ample oportunity for development and progression for our best performers.