
A highly skilled and versatile Senior Research Nurse with a strong foundation in surgical, outpatient, and urology nursing, complemented by hands-on current experience in clinical research. Over the years, I have developed a deep understanding of patient care, from pre-operative assessments to post-operative recovery, with a particular focus on urological conditions. I bring a unique combination of clinical expertise, research-driven insights, and compassionate care, ensuring the delivery of evidence-based practices to improve patient outcomes.
Having worked in diverse healthcare settings, I possess a well-rounded skill set that allows me to manage a variety of patient needs, from surgical cases to routine outpatient consultations. In my role as a research nurse, I have been actively involved in data collection, patient recruitment, and adherence to ethical guidelines, ensuring that research projects progress smoothly while maintaining the highest standard of care for all participants.
I moved into a Senior Research role and this allowed me to further develop my leadership skill where I lead a small team to meet our commitment to the Surgery and Oncology division of our R&D department.
My ability to work effectively in multidisciplinary teams, alongside my commitment to patient safety and education, allows me to contribute meaningfully to both the clinical and research domains. I am passionate about advancing clinical knowledge and improving healthcare delivery through innovative research and patient-centred care. My recent achievements within my Research role at my Trust includes co-ordinating two Research days- 'the Red for Research 2025 day' and the 'Community Open Day'- during which time we hosted a Research stand to create awareness of our Research activity. I have also been the PPIE lead for our trust, to develop equality, diversity and inclusion within the research we conduct.
- Lead Research Nurse for the Surgery and Oncology Portfolio.
- Ensure that the study is conducted adhering to the International Conference for Harmonisation (ICH) and Good Clinical Practise (GCP) guidelines, UK Clinical Trials Regulations and in accordance with its protocol
- Attend Investigator meetings and set up meetings
- Identify and screen for potential research participants
- Be able to advise and support patients and their families when considering participation in a study
- Teach, advise and support medical and nursing staff about the studies so that they can identify, recruit, administer study drugs and care for study patients according to the specific protocol requirements .
- Ensure availability of clear and easy to follow study guidelines, so that staff workload is kept to a minimum
- Participate in the National Institute for Health Research (NIHR) Clinical Research Delivery Network Group Meetings.
- Providing line management and support for R&D Staff working in the Surgery and Oncology division.
- Ensuring that research studies are set up within the required time lines, and that they meet the required time to target.
- Working autonomously, to manage a caseload of patients whilst working as part of a multi disciplinary team. Maintaining effective communication with patients, carers and professionals to ensure high quality service delivery.
- Ensuring patients are fully informed prior to entry into any clinical trial programme and obtaining informed consent.
- Stringent documentation of all aspects from consent through to follow- up, AE and SAE completion.
- Assisting with randomising and the allocation of treatment for patients. Where possible take on the extended role of Principal Investigator.
Evaluate the eligibility of patients for clinical trial entry, co-ordinating pre-study tests, obtaining results and arranging appropriate appointments according to trial protocol. Ensuring my team and I work according to the delegation log as per Principal Investigator.
- Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial.
- Monitor treatment toxicity/ side effects and initiate changes to treatment or treatment cessation as required by trial protocols.
- Perform phlebotomy and cannulation as required by trial protocols, ensure the safe handling, storage and transportation of samples.
- Preparing and co-ordination of monitoring visits.