As a Senior Research Nurse with specialty interest of research transition and Learning Disability, you will lead on the co-ordination and implementation of several research programmes from a variety of different specialities. These research programmes may start in the CRF and transition into the clinical service. Or they may be directly run in the clinical service. You will be accountable for delivery of patient care , clinical research family liaison, ethical recruitment of participants, through facilitating informed consent , administration of the clinical interventions required as part of the study, ensuring the observation ,responding and reporting to side effects ) is undertaken in a timely fashion as well as liaising with research staff in the Trust, drug companies , other study sponsors and ensuring the accurate collection and submission of data, in line with the study protocols and research regulations.
You will manage a caseload of research patients with complex transition and or learning disabilities. You will work alongside the Research Transition Lead nurse to map out patient's journeys on research trials including exit strategies such as compassionate use programmes, post-trial access and managed access programmes. You will advocate and champion for our research patients with learning disabilities and/or Autism to receive the highest possible standard of care throughout their research journey.
The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience and knowledge required. For both documents please view the attachment/s below.
As a Senior Research Nurse with specialty interest of research transition and Learning Disability, you will lead on the co-ordination and implementation of several research programmes from a variety of different specialities. These research programmes may start in the CRF and transition into the clinical service. Or they may be directly run in the clinical service. You will be accountable for delivery of patient care , clinical research family liaison, ethical recruitment of participants, through facilitating informed consent , administration of the clinical interventions required as part of the study, ensuring the observation ,responding and reporting to side effects ) is undertaken in a timely fashion as well as liaising with research staff in the Trust, drug companies , other study sponsors and ensuring the accurate collection and submission of data, in line with the study protocols and research regulations.
You will manage a caseload of research patients with complex transition and or learning disabilities. You will work alongside the Research Transition Lead nurse to map out patient's journeys on research trials including exit strategies such as compassionate use programmes, post-trial access and managed access programmes. You will advocate and champion for our research patients with learning disabilities and/or Autism to receive the highest possible standard of care throughout their research journey.
The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience and knowledge required. For both documents please view the attachment/s below.