Senior Research Nurse
2 weeks ago
Overview
This is an exciting opportunity for a Senior Research Nurse to work in the pioneering world of human-based clinical trials at hVIVO. The role is a full-time, permanent position based between Whitechapel and Canary Wharf.
hVIVO conducts human challenge studies offering services to pharmaceutical and biotechnology companies using various clinical trial methodologies. 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.
The Senior Research Nurse plays a key role in the coordination of clinical unit activities, staff scheduling, and the development of quality service delivery. This includes providing management, support, and guidance to all staff and ensuring a GCP customer-focused service from screening to final study visit.
As a clinical project lead, the Senior Research Nurse is responsible for providing support as a study coordinator on trials and as a line manager for Research Nurses. This role provides mentoring and supervisory support to the clinical team, study support to project teams, and maintains a ward environment conducive to study delivery.
Main Responsibilities
- Leading studies from a clinical perspective from set up to close out of studies;
- Acting as a catalyst for change and improvement in performance quality at a cross-departmental level;
- Hiring, training, and managing Research Nurses and support staff;
- Creating and analyzing metrics towards continuous improvement;
- Quality-focused management, tracking training, and procedural compliance;
- Supervising clinical staff in the clinical environment, providing guidance, and mentoring to Research Nurses and clinical support staff towards clinical excellence;
- Developing and implementing study delivery strategies commensurate with caseload, staff skill mix, and resource;
- Active involvement in process improvements and development of SOPs and other procedural documents;
- Supporting Clinical Operations to ensure the appropriate clinical training is delivered and that desired standards of competency are monitored, maintained, and documented;
- Interpreting health legislation and directives with regard to their impact on or applicability to the Research Environment and ensuring effective implementation as appropriate;
- Ensuring that staff apply current developments in clinical practice;
- Providing input to the hSITE Management Plan and maintaining the hSITE Risk Register;
- Responsible for regular review of hSITE quality systems, driving process change, CAPA completion, and coordinating audit responses;
- Developing strategies to promote staff compliance with process and training.
Requirements
- Solid experience in leading clinical studies from set up to close out in an NHS or commercial setting;
- Good knowledge of Good Clinical Practice and previous experience in a clinical trial setting;
- Ability to work with a degree of flexibility and multi-task;
- Demonstrated leadership and strong motivational skills;
- Previous demonstrable experience of managing the workload of a nursing team;
- NMC Registered;
- Valid Immediate Life Support certification;
- Completed Immunisation and Vaccination (DPC Healthcare providers);
- Excellent time management and organizational skills;
- Good communication skills;
- Sound clinical knowledge;
- Ability to delegate and supervise;
- Ability to prioritize own workload;
- Competence in the recording of medical history, vital signs, ECG, phlebotomy, and the ability and willingness to learn new skills;
- Demonstrated ability to manage a team of clinical professionals and create a productive, satisfying work environment;
- An understanding of ethical practice and confidentiality;
- Good IT skills, including Word and Excel;
- Experience working within the UK healthcare structure for a minimum of 12 months;
- Well-developed knowledge and understanding of clinical supervision.
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