I am a guest speaker and presenter for SBK. These events are organised to support CPD for clinical research staff. My presentations must be current, factual, relatable, easy to follow and valuable to the teams. At the events I answer questions, set group tasks, and ensure that my presentations have actionable take aways for the attendees.

I worked as a EPR training facilitator. This implementation straddled two softwares; Cerner and PBRC for billing and insurance. I supported patient mapping and the design and testing of bespoke workflows for all clinical and non-clinical roles. I was responsible for the creation of lesson plans, quick reference guides, and other learning aids and coordinated e-learning content.

- I managed the Clinical Research Network (CRN) team to ensure that we continued to achieve and surpass our recruitment targets with cancer trials. I prepared and delivered presentations for Research Leads. I implemented time saving, organisational processes, provided training for our team and developed accurate user- friendly source data worksheets for all trials.- During the COVID 19 pandemic, my main priority was to facilitate the opening and execution of COVID 19 vaccine trials to be… Show more - I managed the Clinical Research Network (CRN) team to ensure that we continued to achieve and surpass our recruitment targets with cancer trials. I prepared and delivered presentations for Research Leads. I implemented time saving, organisational processes, provided training for our team and developed accurate user- friendly source data worksheets for all trials.- During the COVID 19 pandemic, my main priority was to facilitate the opening and execution of COVID 19 vaccine trials to be run in the new Clinical Research Facility. This required a comprehensive knowledge of the protocols and study design to enable the trials to be conducted correctly and efficiently. I sourced and trained staff for the recruitment, blinded and unblinded teams. The cohort were healthy volunteers, so different methods were utilised adhering to frameworks, such as volunteer databases and mailing lists. All interest followed up with a screening telephone call to assess and confirm eligibility.-Clinical aspects of my role which includes tissue sample collection and venepuncture.-The department covered trials in many tumour groups gave me the opportunity to expand my knowledge and required me to be versatile due to the variety of trials and studies on the portfolio. I worked with the Research Nurses, Principal Investigators and Medical Teams to identify and screen eligible patients. Once identified I would approach potential research patients via telephone or face to face. I’d introduce and explain the trial, why they have been considered as eligible, what their participation would involve and answer any questions they may have. My delegated responsibilities included taking Informed consent from patients for all non-Clinical Trial Investigational Medicinal Product (CTIMP) studies, registration, randomisation, follow up scheduling, data entry and recruitment log maintenance. Show less

I coordinated a trial looking at the benefits of conservative treatment for patients with bowel cancer. - I was responsible for organising appointments within very tight time frames to suit the trial guidelines. - Reading and interpreting medical imaging and biopsy reports and completing Case Report Forms. - Liaising with patients and doctors to ensure data completeness

- I worked closely with patients to monitor and record their progress, whilst receiving research treatment for lung cancer. - Tasks included questionnaire completion, lung capacity testing, ECGs and consenting. - I also worked in tissue collecting and processing in the lab. Accurate data collection and correct labelling are vital to this role.- I organised clinics and assisted the Doctors and research nurses in the research appointments. - I designed workable timepoint… Show more - I worked closely with patients to monitor and record their progress, whilst receiving research treatment for lung cancer. - Tasks included questionnaire completion, lung capacity testing, ECGs and consenting. - I also worked in tissue collecting and processing in the lab. Accurate data collection and correct labelling are vital to this role.- I organised clinics and assisted the Doctors and research nurses in the research appointments. - I designed workable timepoint specific source data collection sheets, ensuring that they were within R&D, GCP and sponsor legal regulations Show less

- I attended meetings to identify potential patients eligible for clinical research trials. - I worked closely with doctors to streamline and accurately record their data in order enter it onto online systems for analysis. - I organised office space and meetings with external monitors, to assist in cleaning and filtering data

I managed the day to day running of NSHLG (National Study of Hodgkin Lymphoma Genetics). My main responsibilities were to maintain study files, ship supplies to participating sites, develop spreadsheets and data collection methods. I also managed the storage, recording and processing of blood samples.