Venn Life Sciences,  part of hVIVO, 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 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 services 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 looking for a Medical Writer to join our team. Based in our office in Breda, the Netherlands, the role holder will be responsible for the medical writing activities within a clinical trial or project. This may include responsibility for medical writing activities outsourced to third parties.

hVIVO are seeking a Development Scientist to join our team of scientists who are responsible for the development and validation of molecular, virology 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.

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.

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).

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.    The Principal Investigator (PI), at hVIVO is an experienced research physician who provides leadership and direction to the clinical staff during the conduct of a clinical study. A senior role within both the Volunteer Screening Department & Viral Challenge Unit, the PI provides input into the development and management of a clinical study, in addition to carrying out study specific medical duties and screening functions.   Working closely with the Clinical Site Management, other SI’s & the team of Investigators, the PI oversees the study subjects, participates in assessments for eligibility, medical case reviews and medically supervises subjects during screening, out patient studies and within the viral challenge unit. In addition, this requires working across the board with other clinical colleagues, the clinical operations team and project management team.    

This is an exciting opportunity for a 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.    We currently require Bank staff with good availability Monday-Sunday to work a minimum of 2 shifts per week. Shift patterns available are as follows: - 0730 – 1530 (AM shift) - 1230 – 2030 (PM shift) - 0800 – 1600; 0900 – 1700 or 1000 - 1800 (screening day shift) - 1930 – 0830 (Night shift)   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 (clinically vulnerable and shielding) when considering to apply for this role.  

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 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 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.    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 (clinically vulnerable and shielding) when considering to apply for this role.