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Research Coordinator

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Torbay and South Devon NHS Foundation Trust

11d ago

  • Job
    Full-time
    Junior & Mid Level
  • Research & Development

AI generated summary

  • You must support safe research conduct, manage data, coordinate approvals, maintain records, and liaise with organizations, while working across various clinical sites.
  • You will coordinate research studies, ensure regulatory compliance, manage data, maintain documentation, and support trial administration while liaising with various organizations and team members.

Requirements

  • To support the safe conduct of research in accordance with the Research Governance Framework and Good Clinical Practice guidelines and support research in a variety of clinical specialties and departments
  • To provide administrative support and data management for all aspects of trial organisation, as an integrated member of the clinical research team, co-ordinating a variety of clinical research studies, primarily based in TSDFT but may involve working across the community
  • You may be required to travel and work at other sites across the area
  • This role is part of the developing Southwest Peninsula Clinical Research Network and therefore the post holder will be functioning within the Local Research Network structure which is overseen nationally by the Southwest Peninsula Local Research Network (SWPCRN) under the umbrella of the NIHR CRN
  • Assist the Clinical Research and Central R&D teams in co-ordinating a portfolio of studies both within the Trust and across the wider area, working closely with the Lead Research Nurse
  • Co-ordinate all research submissions and amendments and other required approvals, as per Good Clinical Research Practice guidelines (GCP) and in accordance with Research Governance and other regulatory requirements
  • Take a proactive role in the Local Research Network as appropriate and liaise with the Research Network manager/ Lead Nurse and colleagues throughout the network to work towards network aims and objectives and contribute information as appropriate
  • Ensure that both electronic and paper site files for studies are maintained according to regulatory requirements and data is provided promptly to Sponsors and other relevant research staff
  • Undertake accurate data entry using computerised and / or paper-based systems, including support of screening registers where appropriate
  • Keep electronic filing and data systems up to date with accurate information on studies
  • Liaise with various UK organisations in prompt collection of appropriate documentation for research and development and other approvals

Responsibilities

  • To support the safe conduct of research in accordance with the Research Governance Framework, and for clinical trials in accordance with the International Conference on Harmonisation – Good Clinical Practice (ICH – GCP) guidelines and to provide assurance that the rights, safety and well-being of trial participants are protected.
  • To provide administrative support and data management for all aspects of trial organisation, as an integrated member of the clinical research team, co-ordinating a variety of clinical research studies, primarily based in TSDFT but may involve working across the community. You may be required to travel and work at other sites across the area.
  • Assist the Clinical Research and Central R&D teams in co-ordinating a portfolio of studies both within the Trust and across the wider area, working closely with the Lead Research Nurse
  • Co-ordinate all research submissions and amendments and other required approvals, as per Good Clinical Research Practice guidelines (GCP) and in accordance with Research Governance and other regulatory requirements
  • Take a proactive role in the Local Research Network as appropriate and liaise with the Research Network manager/ Lead Nurse and colleagues throughout the network to work towards network aims and objectives and contribute information as appropriate
  • Ensure that both electronic and paper site files for studies are maintained according to regulatory requirements and data is provided promptly to Sponsors and other relevant research staff
  • Undertake accurate data entry using computerised and / or paper-based systems, including support of screening registers where appropriate
  • Keep electronic filing and data systems up to date with accurate information on studies
  • Liaise with various UK organisations in prompt collection of appropriate documentation for research and development and other approvals

FAQs

What is the main purpose of the Research Coordinator position?

The main purpose of the Research Coordinator position is to support the safe conduct of research in accordance with the Research Governance Framework and Good Clinical Practice guidelines, while coordinating a variety of clinical research studies.

Where is the Research Coordinator role based?

The Research Coordinator role is based in the Research and Development Department at the Horizon Centre in Torbay Hospital.

Will the Research Coordinator need to travel for the job?

Yes, the Research Coordinator may be required to travel and work at other sites across the area as part of their duties.

What kind of studies will the Research Coordinator be involved with?

The Research Coordinator will be involved with coordinating a portfolio of clinical research studies across various specialties and departments within the Trust and the wider area.

What regulatory guidelines must the Research Coordinator adhere to?

The Research Coordinator must adhere to the Research Governance Framework and Good Clinical Practice guidelines, as well as the International Conference on Harmonisation – Good Clinical Practice (ICH – GCP) guidelines for clinical trials.

Who will the Research Coordinator collaborate with?

The Research Coordinator will work closely with the Lead Research Nurse, the Clinical Research and Central R&D teams, and colleagues throughout the Local Research Network and other UK organizations.

What types of tasks will the Research Coordinator perform related to data management?

The Research Coordinator will undertake accurate data entry using computerised and/or paper-based systems, maintain electronic and paper site files for studies, and keep data systems up to date with accurate information on studies.

Who should I contact for more information or an informal visit regarding this position?

For further details or to arrange an informal visit, you can contact Lucy Clark, the Lead Research Admin Co-Ordinator, via email at lucy.clark51@nhs.net or by telephone at 01803 656617.

Is prior experience in clinical research required for this role?

The job description does not explicitly state the requirement for prior experience, but it is implied that familiarity with Good Clinical Practice guidelines and research governance would be beneficial for this role.

Are there opportunities for professional development in this position?

As part of the developing Southwest Peninsula Clinical Research Network and under the NIHR CRN umbrella, there may be opportunities for professional development and contribution to the network's aims and objectives.

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Torbay and South Devon NHS Foundation Trust

Better health and care for all

Science & Healthcare
Industry
5001-10,000
Employees
1948
Founded Year

Mission & Purpose

Torbay and South Devon NHS Foundation Trust is a healthcare organisation in the UK that provides a wide range of medical and community services. This includes hospital care, community health services, adult social care, and mental health support across Torbay and South Devon. The Trust's mission is to deliver high-quality, compassionate care, ensuring patients and their families receive seamless, integrated support. Their purpose is to improve the health and well-being of the local community by offering personalised, patient-centred care.