Research Nurse Bank
4 weeks ago
About the Role
This is an exciting opportunity for a part-time bank research nurse to support the Clinical Trial Centre with day-to-day planning and execution of clinical studies screening.
hVIVO conducts human challenge studies, offering services to pharmaceutical and biotechnology companies using a range of different clinical trial methodologies across various 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.
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.
Main Responsibilities
- Administer IMP to volunteers
- Maintain and promote the safety and wellbeing of all subjects participating in a clinical trial
- Assist the senior team with the daily management and allocation of workload
- Prepare, plan, and execute daily clinical activities
- Provide guidance and mentoring to staff in the clinical environment
- Supervise new ancillary staff in the clinical environment as required
- Promote and adhere to Company SOPs, protocols, and Health and Safety Regulations
- Support Clinical Support Specialists in performing clinical assessments
- Perform nurse-specific procedures as identified within the protocol
- Perform informed consent procedures as identified in the study protocol
- Complete study-related documents
- Adhere to Company SOPs, protocols, and Health and Safety Regulations
- Use expertise to input into the development of SOPs and other procedural documents
- Maintain subject safety at all times
- Respond to emergencies as per internal SOP and national guidelines and protocols
- Monitor and identify the deteriorating subject, with appropriate escalation
- Responsible for the checking of emergency resuscitation equipment
- Responsible for maintenance of medicines management within the clinical department
- Supervise clinical staff in the screening unit as delegated by the Senior Research Nurse
- Identify areas for service improvement
Requirements
- IMP dosing experience in research is essential
- Knowledge of GCP and previous experience in a clinical trials setting is essential
- Nursing qualification is essential
- NMC registration is essential
- Completed Immunisation and Vaccination (DPC Healthcare providers)
- Certificate in basic or intermediate life support is essential
- Sound clinical knowledge
- Competence in the recording of medical history, vital signs, ECG, phlebotomy, etc
- Good patient communication skills
- Ability to work within the team
- Good time management skills
- Effective organisational skills
- Ability to work with a degree of flexibility
- Ability to prioritise own workload
- Competence in the recording of medical history, vital signs, ECG, phlebotomy, and the ability and willingness to learn new skills
- Ability to manage adverse events or clinical incidents
- An understanding of ethical practice and confidentiality
- Good IT skills, including Word and Excel
- Strong and demonstrated attention to detail
- Good knowledge of ICH-GCP and regulatory standards
- Willingness to learn additional skills
- Ability to work independently and within the team
- Positive and supportive team player
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