hVIVO is looking for a tech enthusiast to join our team and kickstart their career in the exciting world of IT.   The role is IT Support Apprentice and will be part of a team of experienced Support Enginners. The role will be providing crucial technical support to our London office users.   In this role, you'll embark on an incredible journey where you'll take on diverse responsibilities such as offering first-line support for various systems, keeping our software running smoothly, monitoring daily operations, documenting IT support requests, and even getting hands-on experience in assembling desktops and configuring mobile phones.   This role is site based in our office in E1 (Whitechapel/Aldgate East)  

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 in Whitechapel, E1.   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.      

hVIVO are currently seeking for a QA Manager to join our QA team to work at our London sites in London, E1.      Responsible for overseeing the Management of Quality Assurance Audits conducted by the QA auditing Team and ensuring that procedures performed within the company are in compliance with the relevant SOPs, regulations and internationally recognised guidelines (including Statutory Instrument 2004 No. 1031 its amendments, ICH GCP and GCP for laboratories).

If you have exceptional customer service skills, a healthcare background and are interested in learning more about clinical trials, this is a fantastic opportunity to join our FluCamp team as Clinical Support Specialist at our site in London, E1.   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.   As a Clinical Support Specialist you will perform clinical assessments taking vital signs, ECG’s, venepuncture & spirometry as well as sample and data collections all in accordance with current regulatory requirements, promoting the wellbeing of the volunteer and supporting them throughout participation in the study.   You will provide support and work collaboratively with the team in daily activities within volunteer screening clinic and the Clinical trials quaratine unit.   We currently require a commitment to full time hours. We are a 24/7 operation and shifts available are Mon-Sun, day & night shifts. Flexibility is important. The role will be offered on a zero hours contract at £11. You will be employed via a third party agency.

This is an excellent opportunity to join the the FluCamp Admin team based at our site in London, E1.   Flucamp (a part of hVIVO), conduct 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 our amazing volunteers, in a safe, controlled, clinical environment.   The Clinic Administrator will provide essential administrative support to the clinical team within our busy screening clinic and quarantine clinical trial unit, and for managing the volunteer journey admission and discharge.   This is a Bank position paying £11/hour. We currently require acommitment to full time availability. Shifts will range from 0830 - 1800 with the potential some occasional weekend work so some flexibility is required.    You will be employed via a third party agency and not directly with hVIVO.

This is an excellent opportunity to join the the FluCamp Admin team based at our site in London, E1.   Flucamp (a part of hVIVO), conduct 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 our amazing volunteers, in a safe, controlled, clinical environment.   The Clinic Administrator will provide essential administrative support to the clinical team within our busy screening clinic and quarantine clinical trial unit, and for managing the volunteer journey admission and discharge.   This is a full-time, permanent position. Shifts will range from 0830 - 1800 with the potential some occasional weekend work so some flexibility is required.   

Venn Life Sciences is op zoek naar een Financial Assistant, Breda   Ben jij een financiële professional die zich graag verder wil ontwikkelen in een mooie organisatie die jou veel flexibiliteit en ruimte voor eigen inbreng biedt? Dan is dit de perfecte kans voor jou!   Zal de succesvolle kandidaat mede verantwoordelijk zijn voor tijdige en accurate uitvoering van de financiële transacties, het aanleveren van betrouwbare financiële informatie aan interne en externe belanghebbenden en het verzorgen van de gehele administratie van de Nederlandse vestigingen.   Over Venn Life Sciences Geneesmiddelen zijn niet uit ons leven weg te denken, maar nog steeds zijn er ziektes waarvoor geen goede behandeling bestaat. Farmaceutische bedrijven zijn dan ook druk bezig nieuwe geneesmiddelen te ontdekken, die natuurlijk bij de mens uitgetest moeten worden. Venn Life Sciences is een partner voor bedrijven die nieuwe geneesmiddelen ontwikkelen, door hen te ondersteunen met onze specialistische kennis.   Onze visie is om een centrale rol te spelen in de ontwikkeling van nieuwe producten die ziektepreventie en -behandeling mogelijk maken. We doen dit door een omgeving te creëren die kansen genereert voor werknemers om hun potentieel uit te breiden en hun talenten volledig uit te oefenen, waardoor ze consequent uitstekende service bieden aan onze klanten. We koesteren een omgeving van respect, professionele activiteit, teamwork en houden vooral de patiënt centraal in wat we doen.   Wat bieden wij je aan? Afhankelijk van je opleiding en eerder opgedane werkervaring ontvang je een salaris tussen de € 3.000,- en de € 3.350,-; Goede secundaire arbeidsvoorwaarden zoals een premievrij pensioen, een aanzienlijke compensatie voor ziektekostenverzekering en een winstdelingsregeling; Als voorstander van een goede balans tussen werk en privé bieden wij de mogelijkheid tot parttime werken (minimaal 32 uur) en flexibele werktijden; De mogelijkheid tot thuiswerken. Hiervoor ontvang je een thuiswerkvergoeding en we helpen je bij het inrichten van je thuiswerkplek.   Solliciteren op de vacature Financial Assistant? Stuur je CV naar careers@vennlife.com. Even geen actueel cv bij de hand? Geen probleem! Stuur alleen je contactgegevens en wij bellen jou! De werving en selectie voor deze vacature doen wij in eigen beheer en zijn niet op zoek naar dienstverlening door externe Werving & Selectie bureaus. 

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 hVIVO plc, is an integrated drug development partner offering a unique combination of pre-clinical and CMC drug development expertise with clinical trial design and trial management. This enables us to create, plan and execute drug and medical device development programs effectively and seamlessly for our clients.   Our vision is to deliver results of the highest quality to our global sponsors on time and within budget. We do this through developing our staff to be world class in their fields and forming real, lasting relationships with our clients.   We are looking for a Project Manager Biosample Operations to join our team and be a member of our clients’ international study teams.   You will be responsible for the global coordination and logistics of human clinical samples (biosamples) in a fast-paced and complex international setting with internal and external interfaces in compliance with regulatory requirements and Good Clinical Practice (GCP). Your tasks will include designing, planning, executing, coordinating, and monitoring all logistic aspects and activities (collecting and handling samples, shipments, storage, and data reconciliation) regarding all biosamples for various areas (pharmacokinetics, biomarkers and biobanking). This role concerns a responsibility for biosample management activities outsourced to third parties.  

hVIVO are currently seeking an addition to our Data Entry team to work at our London sites in London, E1.   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 £11/hour. The successful candidate can expect to work full time hours and a good full time availability is required.

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 Patient & 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.   You can find more information about the volunteer journey at FluCamp here: https://flucamp.com/everydayhero/   Patient & Volunteer Experience Co-ordinators screen our volunteers on the phone and confirm their medical history to establish their eligibility for one of our trials. If successful, the volunteers are booked in to attend an in person screening appointment. 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 offering fixed trmcontracts from 30-37.5 hours accross Monday-Friday New starters can expect a full training programme and ample oportunity for development and progression for our best performers. 

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.   The volunteer enrolment marketing manager will be responsible for all activities relating to the development and the day-to-day execution and administration of the marketing plan.   The successful candidate will be responsible for understanding our organisation, key priorities and applying a digital approach to marketing campaigns including content creation and distribution as well as logistical and operational aspects in-person and using digital aspects to enhance community engagement. Attention to detail, ability to manage within a high demand environment, strong interpersonal communications skills, and a focus on execution and results are a must.

hVIVO are seeking a Laboratory Technician to join the Laboratory team at our site in Whitechapel, E1.   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 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. 

Venn Life Sciences,part of hVIVO plc, is an Integrated Drug Development Partner offering a unique combination of pre-clinical and CMC drug development expertise, clinical trial design and management. This enables us to create, plan and execute drug and medical device development programs effectively and seamlessly for our clients.   “Our vision” is to play a pivotal role in the development of new products enabling disease prevention and treatment. We do this by creating an environment that generates opportunities for employees to stretch their potential and fully exercise their talents thereby consistently providing outstanding service to our clients. We nurture an environment of respect, pro activity, teamwork and above all keep the patient at the heart of what we do.   We are currently looking for a senior CMC Consultant with extensive experience in biological drug substance development (e.g., USP, DSP and cell line development) obtained in pharma industryto join our CMC Team based in Breda, The Netherlands. The successful candidate will have the opportunity to work from one of our European offices and/or home with regular visits to our office in Breda.   Reporting to the Head of CMC, the successful candidate will be responsible for providing input and guidance on the design, execution, and coordination of the CMC elements of client projects related to the development of biopharmaceutical compounds.   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 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 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   We are looking to expand our Facilities team with this new position of Facilities Assitant based at our East London site.  You will have a can do, hands on, proactive attitude with the ability to multitask in a fast paced environment.   The position is primarily to cover our London sites in E1 however some travel may be required.

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 number of Bank Study Physicians 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.  

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.  

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.