Clinical Trials Coordinator inManchester inManchester PUBLISHED
TUE 12 NOV 2024
The Christie NHS FT roI7Sm3e
Key responsibilities include managing data, completing case report forms, maintaining site files, invoicing, and liaising with various stakeholders, including research teams and trial sponsors. The role requires strong organisational and communication skills, along with knowledge of clinical trials and Good Clinical Practice (GCP).
The coordinator will assist with trial setup, processing trial amendments, supporting safety reporting, and maintaining readiness for inspections. This position involves collaboration with both internal and external parties, requiring confidentiality and sensitivity. Overall, the role supports the smooth operation of clinical trials within the research division.
Candidates must meet the essential criteria outlined in the job specification, and this position does not offer sponsorship. The application closing date may be adjusted depending on applicant volume.
Please note that this post is offered as a permanent contract at 37.5 h/week.
We are looking to appoint a Clinical Trials Coordinator (Band 4) to the Urology and Head and Neck research teams within The Christie NHS Foundation Trust. The research teams form part of the Research and Innovation division.
We are seeking an enthusiastic, motivated and experienced individual who will be responsible for assisting the research nurses, consultants and trial coordination management team with various aspects of clinical trial administration/ coordination.
We are looking for a candidate with exceptional organisational and communication skills, administration experience and knowledge of clinical trials/GCP.
This role will not meet the requirements of sponsorship. Please note that the closing date of the job may be brought forward if there is a high volume of applicants.
Applicants should meet all the essential criteria within the person specification section of the job description as a minimum.
You will be responsible for data management, case report form completion, site file maintenance, archiving, invoicing, communication with trial sponsors, monitors, and the wider research community, maintaining electronic records to support the team and assisting with the set-up of new studies.
You will liaise with many different members of staff including internal service departments, central R&I office colleagues, clinicians and research nurses, as well as external collaborators, i.e. trial sponsors, monitors and the wider research community, so good communication and interpersonal skills are key.
Please see the attached job description for a more detailed description of the tasks this job will involve.
About us
DUTIES AND RESPONSIBILITIES
The specific responsibilities will depend on the requirements of each team, but may include:
- Act as a point of contact for the Research and Development core team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to general trial conduct.
- Assist with the general administrative duties associated with the set up and initiation of rials within an assigned team, under the supervision of the Senior Clinical Trials Coordinators.
- Assist with completion of activity logs to enable invoices to be raised. Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times.
- Assist with the processing of trial amendment submissions in accordance with ICH- GCP and Trust SOPs and timelines, under the supervision of the Senior Clinical Trials Coordinators.
- Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements, under the supervision of the Senior Clinical Trials Coordinators
- Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas).
- Assist the Clinical Trials Coordinators with the development of trial workbooks for review by the lead Clinical Research Nurse and Principal Investigator.
- Ensure collection of clinical case notes for all patients, so that these are available as needed, for monitoring and audit purposes.
- Complete case report forms as per sponsor requirements and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits. This will be under the supervision of the Senior Clinical Trials Coordinators.
- Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.
- Arrange shipping and delivery of relevant trial data and documents including import/export of tumour blocks, ECGs and copy scans
- Arrange team and trial related meetings as required, producing minutes in a timely manner.
- Ensure that data is available and up to date for any meetings related to a clinical trial in collaboration with the Senior Clinical Trials Coordinators.
- Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary).
- Assist with general preparation for audit and inspections within assigned teams, under the direct supervision of the Senior Clinical Trials Coordinators and lead Clinical Research Nurse.
- Assist with trial document archiving by following the Trusts archiving guidelines.
- Ensure that office/ trial related supplies are adequate and assist with the ordering process.
- Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment teams. Demonstrates the agreed set of values and accountable for own attitude and behaviour.
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