Research Trial Physician
4 weeks ago
Position Overview
hVIVO is at the forefront of human-based clinical trial innovation, aiming to expedite the development of pharmaceuticals and vaccines targeting respiratory and infectious diseases. By utilizing human disease models in conditions such as influenza, RSV, HRV, and other respiratory ailments, our platform captures the progression of disease, providing insights into the entire lifecycle from health to illness and recovery. Our goal is to be the preferred partner for organizations developing airway disease products, facilitating early proof of concept for their efficacy and identifying optimal patient profiles for advanced clinical studies. hVIVO is recognized as a leader in human challenge models globally.
We are seeking several Bank Study Physicians to join our team, who are available for flexible evening and weekend shifts.
In this role, you will be responsible for the screening and evaluation of participants throughout their involvement in the clinical trial process, ensuring that all assessments and procedures adhere to protocol requirements, standard operating procedures (SOPs), and comply with ICH Good Clinical Practice (GCP), along with other regulatory standards.
Key Responsibilities
Clinical Duties
Execute clinical procedures as mandated by the protocol and within your area of expertise. Oversee and assess clinical procedures conducted by other staff, ensuring eligibility and monitoring any changes in clinical conditions. Conduct informed consent processes while upholding ICH GCP standards. Provide clinical guidance and support to the unit's clinical staff. Identify areas for service enhancement and collaborate with senior staff to uphold and elevate standards within the clinical environment.Study Coordination
Support the Senior Study Physician and/or Sub-Investigator with staffing needs and contribute to the overall scheduling of personnel. Review and provide input on study protocols regarding logistical and medical feasibility as requested by senior research personnel. Participate in internal training specific to the study. Document participant information accurately in source documentation and/or case report forms (CRFs) as per study requirements.Participant Management
Ensure informed consent procedures are conducted with participants prior to any procedures. Maintain accurate records of the informed consent process in each participant's documentation. Confirm that participants enrolled in research studies meet eligibility criteria. Gather participant medical histories and medication usage details. Update participant tracking forms and hVIVO databases as necessary. Maintain professional boundaries with participants. Collaborate with cross-functional teams to ensure sample requirements and timelines are met. Safely discharge participants from the study, including necessary documentation to their general practitioners. Report any medical concerns to the senior medical team. Provide out-of-hours emergency coverage as needed.Required Qualifications
Full registration with the General Medical Council (GMC). Medical degree. Current Advanced Life Support (ALS) certification. Proficiency in English. Experience within the UK healthcare system. Skills in phlebotomy and cannulation. Previous post-graduate experience in areas such as internal medicine, general practice, emergency medicine, respiratory medicine, or infectious diseases.Connect with Us
If you are interested in this opportunity, we encourage you to consider joining our innovative team at hVIVO.
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