Clinical Research Fellow in Cardiology
6 months ago
Principal duties of post will involve running of a clinical trial of pacing in patients undergoing cardiac surgery. You will be responsible for identifying suitable trial patients from the in-patient and out-patient surgical waiting lists, co-ordinating their pre-admission investigations, ensuring patients meet the trial inclusion criteria, patient consent, administration of pacing therapies as per trial protocol, daily review of patients and collection of study data (imaging, biochemistry, ECG, haemodynamics), planning patient discharge and follow-up investigations. The trial will also be conducted at the cardiac centre in Morriston (Swansea Bay Hospital) where you will be expected to adopt similar roles.
You will be working closely with your academic supervisor (Professor Yousef) and with cardiac surgeons and anaesthetists involved in the care of patients undergoing cardiac surgery at both study sites.
You will be expected to work closely with the clinical trial management unit in CEDAR to ensure appropriate data collection, documentation, and recording in line with data protection and good clinical practice policies.
Principal duties of post will involve running of a clinical trial of pacing in patients undergoing cardiac surgery. You will be responsible for identifying suitable trial patients from the in-patient and out-patient surgical waiting lists, co-ordinating their pre-admission investigations, ensuring patients meet the trial inclusion criteria, patient consent, administration of pacing therapies as per trial protocol, daily review of patients and collection of study data (imaging, biochemistry, ECG, haemodynamics), planning patient discharge and follow-up investigations. The trial will also be conducted at the cardiac centre in Morriston (Swansea Bay Hospital) where you will be expected to adopt similar roles.
You will be working closely with your academic supervisor (Professor Yousef) and with cardiac surgeons and anaesthetists involved in the care of patients undergoing cardiac surgery at both study sites.
You will be expected to work closely with the clinical trial management unit in CEDAR to ensure appropriate data collection, documentation, and recording in line with data protection and good clinical practice policies.
Cardiff and Vale University Health Board is one of the largest Integrated Health Boards in the UK, employing over 15,000 staff, providing over 100 specialist services. Working across 6 hospital sites, we have a diverse range of career opportunities to offer. Serving around 500,000 people living in Cardiff and the Vale of Glamorgan, we are focussed on the health and care needs of our local population whilst working with our partners to develop regional services.
Our mission is “Caring for People, Keeping People Well”, and our vision is that every person’s chance of leading a healthy life should be equal. As an organisation we are unashamedly ambitious for our population’s health, rising to the challenges of today and tomorrow through our 10-year strategy, Shaping our Future Wellbeing. We are contributing to a healthier Wales with great emphasis placed on innovation and improvement, learning from around the world and leading the way in clinical research. Partnership working is strong at Cardiff and Vale, and we work closely with our staff and our community.
Cardiff, the thriving Welsh capital, is a fantastic city to live and work in with an abundance of sports, arts and cultural attractions. Situated to the west of Cardiff, the Vale of Glamorgan offers a combination of beautiful Welsh countryside and a dramatic natural coastline. Whether city life or rural living, Cardiff and the Vale offers the best of both worlds.
There is no commitment to out of hours work, but there may be opportunities to join the cardiology SpR on-call rota as additional duty.
Principal duties of post will involve running of a clinical trial of pacing in patients undergoing cardiac surgery. You will be responsible for identifying suitable trial patients from the in-patient and out-patient surgical waiting lists, co-ordinating their pre-admission investigations, ensuring patients meet the trial inclusion criteria, patient consent, administration of pacing therapies as per trial protocol, daily review of patients and collection of study data (imaging, biochemistry, ECG, haemodynamics), planning patient discharge and follow-up investigations. The trial will also be conducted at the cardiac centre in Morriston (Swansea Bay Hospital) where you will be expected to adopt similar roles.
You will be working closely with your academic supervisor (Professor Yousef) and with cardiac surgeons and anaesthetists involved in the care of patients undergoing cardiac surgery at both study sites.
You will be expected to work closely with the clinical trial management unit in CEDAR to ensure appropriate data collection, documentation, and recording in line with data protection and good clinical practice po
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