Research Nurse Bank Specialist

6 hours ago

London, Greater London, United Kingdom hVIVO Full time
Overview

This is an exciting opportunity for a part-time Research Nurse to support the Clinical Trial Centre with day-to-day planning and execution of clinical studies. As a Research Nurse, you will work on a specific trial, covering various duties, including administering IMP to volunteers, maintaining and promoting the safety and wellbeing of all subjects, and assisting the senior team with workload management.

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 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
  • 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, such as logs, source data, and CRFs
  • 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, responding to emergencies as per internal SOP and national guidelines and protocols
  • Monitor and identify deteriorating subjects, with appropriate escalation
  • Responsible for checking emergency resuscitation equipment as per SOP/OIs
  • Responsible for maintenance of medicines management within the clinical department as per SOP/OI
  • Responsible for supervision of clinical staff in the screening unit as delegated by the Senior Research Nurse
  • Identify areas for service improvement
  • Promote a high standard of practice and care at all times
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 recording medical history, vital signs, ECG, phlebotomy, etc. is essential
  • Good patient communication skills are essential
  • 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 recording 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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