Clinical trials coordinator at Guys and St Thomas NHS Foundation Trust
London SE1, England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

14 Jul, 25

Salary

53134.0

Posted On

14 Apr, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

We are looking for an enthusiastic and experienced senior research coordinator to join our team on a 12 month fixed term maternity cover basis.
The post holder will be responsible for leading the provision of a full administrative and coordination research service across the Gastrointestinal Medicine & Surgery directorate . They will have a pivotal role in the set up and feasibility of a portfolio of in-house, national and international clinical studies. They will oversee invoicing and research finance for non-commercial research studies. They will coordinate studies in setup and work with the delivery team and R&D to manage protocol amendments.

Responsibilities will include managing research budgets and staff, undertaking study feasibility assessment and leading on public engagement. Further to this the post holder will monitor recruitment processes, implement change where necessary and maintain high standards at all times. The post holder will ensure confidential and sensitive information is kept secure, and that all work will be carried out in accordance with both the Trust’s policies and Good Clinical Practice (GCP) regulations. The post holder will work closely to the GMS Research Matron and R&D Lead, GMS research team and the GSTT R&D teams.

  • Invoicing and financial oversight management
  • Research governance
  • Coordinating and managing a large portfolio of studies in setup
  • Managing amendments
  • Feasibility assessment and support local C&C assessment
  • Overseeing study close down and managing archiving
  • Supporting the research delivery team
  • Leading and overseeing procurement

Guy’s and St Thomas’ NHS Foundation Trust comprises five of the UK’s best-known hospitals – Guy’s, St Thomas’, Evelina London Children’s Hospital, Royal Brompton and Harefield – as well as community services in Lambeth and Southwark, all with a long history of high-quality care, clinical excellence, research and innovation. We are among the UK’s busiest, most successful foundation trusts. We have a long tradition of clinical and scientific achievement and – as part of King’s Health Partners – we are one of England’s eight academic health sciences centres, bringing together world-class clinical services, teaching and research.
Are you a dynamic and motivated clinical trial coordinator?
Are you keen to coordinate clinical research that’s embedded in a busy NHS setting?
Are you organised and a great team player ?
This role will offer the post holder an opportunity to work closely with experienced clinical and research colleagues from across the trust, supporting a varied portfolio of non-commercial research studies. Successful candidates will be brilliant at communication with a range of teams and professionals, able to manage their time well and confident in research governance. Previous clinical research experience is essential. You will be joining an enthusiastic, friendly, and motivated multidisciplinary team in a dynamic teaching hospital in central London, and you will be an essential member of the research team.

Responsibilities

ROLE INCLUDES:

  • Invoicing and financial oversight management
  • Research governance and maintaining GCP
  • Coordinating and managing studies in setup from feasibility to end of study
  • Implementing and managing amendments to existing studies.
  • Feasibility assessment and support local C&C assessment
  • Organising Site Initiation Visits
  • Overseeing study close down and managing archiving
  • Supporting the research delivery team
  • Overseeing procurement and ordering of consumables
  • Acting as main a point of contact for enquires relevant to trial set up.
  • Facilitating governance project board meetings on a monthly basis to discuss new research proposals.
  • Updating EDGE/EPIC with recruitment when needed
  • Confirming recruitment for sponsored studies on CPMS
  • Playing a pivotal role in the monitoring and development of current local Standard Operating Procedures to ensure that they are fit for purpose and accurately detail procedures for study processes.
  • Providing guidance and expertise on research set up, through development of specialist, in-depth knowledge.
  • Working with the Principal Investigators, Research delivery team, R&D and management to ensure the successful set up of new studies.
  • Supporting and guidance to new staff as appropriate in all area of study delivery/governance and provide training where necessary
  • Providing regular updates on the progress of new studies
  • Managing and prioritise their own workload
  • Going through the researcher checklist handbook with new researchers
  • Organisation of Investigator site file prior to sponsor greenlight including version control, localisation, signed delegation logs.
  • Co leading the patient Research Advisory Group
    There are excellent opportunities for further education and leadership development within this role, including training and an individual personal development plan. The normal working hours for the post are 9am-5pm but this can be discussed and there are opportunities for flexible working arrangements. The posts are mainly based at Guys Hospital but there will be cross site travel required to other sites such as St Thomas’ Hospital

Responsibilities will include managing research budgets and staff, undertaking study feasibility assessment and leading on public engagement. Further to this the post holder will monitor recruitment processes, implement change where necessary and maintain high standards at all times. The post holder will ensure confidential and sensitive information is kept secure, and that all work will be carried out in accordance with both the Trust’s policies and Good Clinical Practice (GCP) regulations. The post holder will work closely to the GMS Research Matron and R&D Lead, GMS research team and the GSTT R&D teams.

  • Invoicing and financial oversight management
  • Research governance
  • Coordinating and managing a large portfolio of studies in setup
  • Managing amendments
  • Feasibility assessment and support local C&C assessment
  • Overseeing study close down and managing archiving
  • Supporting the research delivery team
  • Leading and overseeing procuremen
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