Jobs at hVIVO

Provide nursing support for viral-challenge clinical trials: perform clinical assessments and nurse-specific procedures, obtain informed consent, complete CRFs and source data, maintain subject safety and emergency preparedness, manage medicines and resuscitation equipment, supervise screening staff, follow ICH GCP, SOPs and NMC Code, and identify service improvements.

Lead and oversee clinical trial projects end-to-end, ensuring delivery on time, on budget, and to quality standards. Manage cross-functional project teams, line-manage Project Managers, serve as primary client contact, and drive process improvement across the department and company.

Lead clinical delivery of trials from start-up to close-out; act as study coordinator and line manager for research nurses. Provide mentoring, supervise site team, ensure patient safety and regulatory compliance (ICH GCP, NMC), and perform clinical tasks (vitals, ECG, phlebotomy).

Serve as clinical project lead for human challenge clinical trials from start-up to closeout. Provide study coordination, line management and mentorship for research nurses, support project teams, maintain ward readiness, and ensure evidence-based nursing practice and high standards of care.

Lead clinical delivery of phases 1–2 trials from start-up to closeout. Act as clinical project lead and study coordinator, supervise and mentor research nurses, manage daily clinical workload, ensure GCP/ICH compliance, record vital signs, train staff, and prepare study documents (SOPs, logs, source data, CRFs).

Provide medical leadership for clinical studies at the Clinical Trial Centre, perform study-specific medical duties and volunteer screening, manage clinical input to study development, conduct phlebotomy/cannulation, prescribe and manage participant care, and ensure compliance with study and UK healthcare standards.

Perform clinical assessments (vital signs, ECGs, venepuncture, spirometry), screen and schedule volunteers, collect/process/dispatch samples, record temperature monitoring per SOPs, ensure data accuracy, support daily clinic operations, and assist training and supervision of ancillary staff while following ICH-GCP and regulatory standards.

Lead clinical delivery for trials from start-up to close-out. Act as study coordinator and line manager for Research Nurses, providing mentoring, supervision and staff training. Oversee daily clinical activities and workload allocation, ensure evidence-based nursing and ICH-GCP compliance, record vital signs, support Phase I/II trials, and create/review study documents (SOPs, logs, source data, CRFs).

Provide and lead nursing care for clinical trial delivery from start-up to close-out. Act as clinical project lead and study coordinator, supervise and mentor research nurses, ensure subject safety and regulatory compliance (ICH GCP, NMC), and maintain a ward environment conducive to study activities.

Lead and coordinate clinical trial activities from start-up to close-out. Provide nursing care, supervise and mentor research nurses, ensure regulatory compliance (ICH GCP, NMC), perform clinical assessments (vitals, ECG, phlebotomy), and support study teams to maintain a ward environment conducive to study delivery.

Lead and oversee clinical trial projects end-to-end, ensuring delivery on time, on budget, and to quality standards. Manage cross-functional teams, line-manage Project Managers, act as primary client contact, and drive departmental process improvements.

Senior research physician providing medical leadership for clinical trials using the human viral challenge model. Oversees subject screening, outpatient and in-unit medical management, trial design input, staff training, GCP compliance, IMP handling, and clinical documentation.

Provide clinical nursing care and coordinate clinical trial delivery from start-up to close-out. Act as clinical project lead and study coordinator, supervise and mentor research nurses, ensure GCP and regulatory compliance, perform clinical assessments (vitals, ECG, phlebotomy), and maintain a ward environment supportive of study activities.

Lead clinical delivery of trials from start-up to close-out as study coordinator and line manager. Provide nursing care, supervise and mentor research nurses, ensure participant safety under ICH GCP and NMC Code, perform clinical assessments (history, vitals, ECG, phlebotomy), and maintain a ward environment conducive to study delivery.

Provide nursing services to support clinical trial delivery, acting as clinical project lead from start-up to close-out. Coordinate studies, supervise and mentor research nursing staff, ensure participant safety and regulatory compliance (ICH GCP, NMC Code), perform clinical assessments (medical history, vitals, ECG, phlebotomy), and maintain a ward environment conducive to study delivery.

Senior research physician providing clinical leadership for human viral challenge studies. Oversees medical management, screening, protocol input, IMP handling, staff training/mentoring, GCP compliance, CRF/source documentation review, and contributes to study design, consent, logistics, and reporting.

Provide nursing care and support for early phase clinical trials, including screening, quarantine, informed consent, clinical assessments, specimen collection, monitoring safety, emergency response, documentation, and supervision of clinical staff, ensuring compliance with GCP, NMC, SOPs and study protocols.

Provide nursing support for clinical trials at the London site, assisting with day-to-day planning and execution of studies, including participant screening and quarantine management.

Lead clinical delivery for trials from start-up to close-out, acting as study coordinator and line manager for research nurses. Provide mentorship, supervise daily clinical activities, ensure ICH-GCP compliance, maintain evidence-based nursing standards, manage workload allocation, train staff, and prepare study documentation including SOPs, source data, logs, and CRFs for phase 1 and 2 trials.

Manage volunteers through screening, quarantine, and follow-up; act as primary contact, liaise with GPs and clinicians, ensure protocol and ICH/GCP compliance, handle payments and travel arrangements, perform reception duties, and protect confidentiality.