Senior Clinical Trial Coordinator

3 weeks ago

Bristol, United Kingdom University Hospitals Bristol And Weston Nhs Foundation Trust (Uhbw) Full time

Job summary An exciting opportunity has arisen within the evolving Clinical Research Unit (CRU) at the Bristol Eye Hospital.
We are looking to appoint an enthusiastic individual as a Senior Trial Coordinator.The post holder will be in contact with a broad professional group, as well as members of the public and research sponsors, therefore excellent communication, interpersonal and organisational skills are paramount.We are seeking a flexible, motivated team player with considerable nursing experience and an interest and enthusiasm for research.Experience in clinical research is required and ophthalmology experience would be advantageous.
The post holder will be an integral member of the CRU senior team, involved in the line management, support and training of staff as well as more complex trial developments, including early phase and advanced therapy trials.
Main duties of the job Working closely with the Clinical Research Unit Manager and as a member of the senior team, the post holder will support colleagues and researchers throughout the research process, including the delivery of some clinical aspects associated with our protocols.The postholder will be responsible for line managing junior members of the coordination team and will be expected to demonstrate leadership skills.You will manage an ongoing portfolio of studies, (including more complex trials such as early phase trials), performing a variety of tasks such as completing case report forms, maintaining study documentation, processing amendments, and planning and organising patient appointments.A component of this role is the requirement to perform some clinical work, for example, including assisting in the informed consent procedure, venepuncture, vital signs, urine testing and ECGs.
Full training will be given, with an opportunity to gain accreditation as a Clinical Research Practitioner, which is now identified as an occupational group in health and care in the UK by the UK Professional Standards Authority (PSA).Training and development features high on our list of priorities.Therefore the post holder will be a flexible, motivated team player willing to further develop their understanding of clinical trials.
About us University Hospitals Bristol and Weston NHS Foundation Trust (UHBW) is one of the largest acute Trusts in the country, bringing together a combined workforce of over 13,000 staff and over 100 different clinical services across 10 different sites, serving a core population of more than 500,000 people across South West England.
UHBW has been rated by the CQC as 'Good' overall and our staff are proud to deliver excellent care to the people of Bristol, Weston and beyond.
As a forward- thinking multi-award winning Trust and a digital exemplar committed to improving patient care, our world-leading research and innovations are having a positive local and global impact.
Our hospitals are spread across Bristol and Weston, join us and you can enjoy the very best of both worlds; city living within a stone's throw of the countryside or beside the seaside, both with easy access to all that the South West has to offer.
UHBW is committed to safeguarding and promoting the welfare of children, young people and vulnerable adults.
As an equal opportunities employer actively working towards a diverse workforce we aim to recruit and retain a workforce which represents the rich diversity of the local population at all levels and are committed to designing our services around the needs of individual patients and those around them.
Anonymous information will be used from your application in order to ensure we're meeting our pledge.
Job description Job responsibilities Please refer to the Job description and person specification for details of the main responsibilities for the role.
Person Specification Knowledge and Experience Essential Recent and significant clinical research experience in NHS / academic / pharmaceutical setting Previous research data management experience Previous experience of medical terminology Ability to demonstrate an understanding of, and previous experience of the clinical research process, ICH-GCP and research governance Qualifications and Training Essential Degree in health/research related subject or substantial relevant experience Current ICH GCP Skills and Abilities Essential Good IT skills.
Proven ability to use Microsoft Office and related packages, including databases, spreadsheets.
Reliable and capable of working with confidential and sensitive information Ability to plan, manage, adjust, and deliver complex projects, involving multiple agencies and individuals and a broad range of activities, to tight deadlines Strong problem-solving skills Excellent organisational and interpersonal skills To be able to prioritise workload Desirable Good understanding of workforce planning Experience of leading teams Ability to prepare and deliver presentations and reports to a high standard

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