An opportunity has arisen for a Research Coordinator in the Research and Development Department based in the Horizon Centre at Torbay Hospital.
You will work 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 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.
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
The Research and Development Department works to support the safe conduct of research in accordance with the Research Governance Framework and Good Clinical Practice guidelines.
We work across the organisation, supporting research in a variety of clinical specialties and departments.
We provide expertise from setting up studies to support, facilitate and provide guidance on the administration of the compliance and other related aspects of the clinical study.
Why Work With Us
Coordinate (under supervision of research practitioners) protocol generated assessments, questionnaires and diaries and provide information on trials to medical personnel/multi-disciplinary team
Assist the research team in maintaining computer systems for managing the local Network portfolio of studies and providing annual reports
Be responsible for complex data collection on a specific portfolio of studies as per Good Clinical Research Practice guidelines (GCP)
Able to receive, handle, analyse and resolve data queries promptly. Direct unresolved queries to appropriate team member
Be able to prioritise workload when frequently interrupted
Assist teams in preparation of accurate trial reports and presentations
Be able to respond to patients/carers telephone calls (who may at times be distressed) tactfully and empathetically
Respond quickly and appropriately to all enquiries and queries, directing to most appropriate team member
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