hVIVO - Whitechapel

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Venn Life Sciences, part of Open Orphan 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 Clinical PK/PD Data Analyst to join Clinical PKPB Team based in our office in Breda, Netherlands. Reporting to the Group Leader Clinical Pharmacokinetics, the successful candidate will be responsible for independently managing a diverse and complex range of non-compartmental (NCA) pharmacokinetic and pharmacodynamic analysis of a clinical trial. The role holder will support the consultants in clinical pharmacokinetics / clinical development.  If you are seeking a rewarding and challenging career this could be the perfect opportunity for you.
iCIMS ID
2022-2651
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.  
iCIMS ID
2022-2645
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 company is expanding and looking to strengthen the Business Development Team with a Business Development Coordinator, who can be completely field based. 
iCIMS ID
2022-2644
hVIVO is part of Open Orphan,a rapidly growing niche CRO pharmaceutical services company which is a world leader in the testing of vaccines and antivirals through the use of human challenge clinical trials. The company has a leading portfolio of 8 viral challenge study models, 2 FLU, 2 RSV, 1 HRV, 1 Asthma, 1 cough and 1 COPD, with a COVID-19 model under development.  This is a very exciting time and we are expanding our teams in the UK and are interested to hear from similarly dynamic  individuals who share our vision to better understand the more precise nature of human disease and to really make a difference.
iCIMS ID
2022-2643
Venn Life Sciences,part of Open Orphan 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 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 study or project. This may include responsibility for Medical Writing activities outsourced to third parties.
iCIMS ID
2022-2640
Venn Life Sciences,part of Open Orphan 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 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 Clinical Biosample Operation Expert 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) independently. This role concerns a responsibility for biosample management activities outsourced to third parties. 
iCIMS ID
2022-2639
Venn Life Sciences,part of Open Orphan 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 an expert in Advanced Therapeutic Medicinal Products (ATMPs), to join our CMC Consultancy Team based in Breda, The Netherlands. You will have the opportunity to work from one of our European offices and/or home with regular visits to our office in Breda. You will work for clients but will also work together with the CMC team. We share knowledge and information and help each other where needed. This way you will be involved in/exposed to many projects.  The successful candidate has experience in the manufacturing & analysis of ATMPs and its regulations. The candidate is a team player and would like to help the team to develop further into the field of ATMPs. 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 ATMPs and other biological products.  If you are seeking a rewarding and challenging career, being a consultant and being part of a team of experts, this could be the perfect opportunity for you.
iCIMS ID
2022-2638
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. For our Marketing Manager role, we are seeking an energetic and organised person to join the patient and volunteer enrolment team at hVIVO based in London.
iCIMS ID
2022-2628
Venn Life Sciences (part of the Open Orphan 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, Randomization and Regulatory Affairs. We have dedicated operations in France, the Netherlands and the UK.  Venn Life Sciences biometry offers a unique set of high quality, innovative data management and biostatistics services utilising 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 Junior Statistical SAS programmer to join our team in September 2022. The position will be based in Paris, France and will report to the Head of Biostatistics.
iCIMS ID
2022-2627
Venn Life Sciences biometry offers a unique set of high quality, innovative data management and biostatistics services utilising 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 Statistical SAS programmer to join our team in September 2022. The position will be based in Paris, France (Homebased possible according to profile) and will report to the Head of Biostatistics.
iCIMS ID
2022-2626
We have an exciting opportunity, as we are expanding and are currently seeking a SAS Programmer ( CDISC, SDTM ) to join our Data Management team. The Office is based in Paris, France but hybrid / homebased is possible. Venn Life Sciences biometry offers a unique set of high quality, innovative data management and biostatistics services utilising 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. Its a great team, so if you feel your skills match below, then please reach out and apply.
iCIMS ID
2022-2625
Venn Life Sciences is an Integrated Drug Development Partner offering a unique combination of drug development expertise and 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. We have dedicated operations in Ireland, France, the Netherlands, the UK, the US, and Europe-wide representation. "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." You are part of a team of Scientific Monitors, who support the our clients drug development programs by setting up and monitoring external biomarker analysis supporting clinical studies for  drug development. Your contribution is essential to achieve a comprehensive, high-quality biomarker data set, useful to generate new information about the drug concept and drug activity and finally to support data driven decision making in clinical projects. Furthermore, you contribute to the overall adherence to the quality and compliance with regards to outsourced biomarker analysis.
iCIMS ID
2022-2600
Venn Life Sciences is an Integrated Drug Development Partner offering a unique combination of drug development expertise and 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. We have dedicated operations in Ireland, France, the Netherlands, the UK, the US, and Europe-wide representation. "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 currently looking for a Consultant Clinical Pharmacokinetics to join Clinical Development Team based in our office in Breda, Netherlands. Reporting to the Group Leader Clinical Consultancy, the successful candidate will be responsible for providing expertise regarding the design, initiation and coordination of the Clinical Pharmacokinetic elements of the study or part of a project in a timely manner with high quality awareness If you are seeking a rewarding and challenging career this could be the perfect opportunity for you.
iCIMS ID
2022-2587