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Clinical Research Physician
3 months ago
Position Overview
hVIVO is at the forefront of innovative clinical trial methodologies, focusing on expediting the development of therapeutics and vaccines for respiratory and infectious diseases. Utilizing human disease models in influenza, RSV, HRV, and other respiratory conditions, our platform provides a comprehensive view of disease progression, from health to illness and recovery. Our goal is to be the preferred collaborator for organizations aiming to validate their products in airway diseases, facilitating early proof of concept and identifying optimal patient profiles for advanced clinical trials. hVIVO is recognized as a leader in human challenge studies.
We are seeking qualified Bank Study Physicians to join our team, 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 regulatory guidelines, including ICH GCP and GMC standards.
Key Responsibilities
Clinical Responsibilities
- Execute clinical procedures as outlined in the protocol, ensuring competency.
- Oversee and assess clinical procedures performed by other staff, monitoring eligibility and changes in clinical conditions.
- Conduct informed consent processes while upholding ICH GCP standards.
- Provide clinical guidance and support to unit staff.
- Identify areas for service enhancement and collaborate with senior staff to elevate clinical standards.
Study Coordination
- Assist the Senior Study Physician and/or Sub-Investigator with staffing needs and overall staff scheduling.
- Review and contribute to study protocols regarding logistical and medical feasibility as requested.
- 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 completed prior to participant involvement in any procedures.
- Maintain accurate records of informed consent in each participant's documentation.
- Verify participant eligibility for research studies.
- Collect comprehensive medical histories and medication usage from participants.
- Update participant tracking forms and hVIVO databases as necessary.
- Maintain professional boundaries with participants.
- Collaborate with cross-functional teams to meet sample requirements and timelines.
- Ensure safe discharge of participants from the study, including necessary documentation to their general practitioners.
- Report any medical concerns to the senior medical team.
- Provide emergency cover as needed outside of regular hours.
Required Qualifications
- Full GMC registration.
- Medical Degree.
- Current ALS certification.
- Proficiency in English.
- Experience within the UK healthcare system.
- Skills in phlebotomy and cannulation.
- Relevant post-graduation experience in fields such as internal medicine, general practice, emergency medicine, respiratory medicine, or infectious diseases.
Connect With Us
For those interested in future opportunities, we welcome general inquiries.
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