Clinical Trials Coordinator | The Christie NHS Foundation Trust - Manchester - ref. j28849015
The main purpose of the role is to provide comprehensive data management and administrative support to the Lung Clinical Trials Team according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies.
The successful post holder will have experience working within clinical trial delivery within an NHS site and preferably an understanding of oncology research.
The post holder will:- Manage and maintain the clinical trials database.
- Assist with the efficient and timely set up of clinical trials.
- Assist with the tracking and raising of invoices.
- Provide support with maintenance and quality assurance of all trial related documentation in accordance with relevant legislation and guidelines.
- Assist with preparation for audit and inspections within assigned teams.
- General trial-related communication in accordance with the Data Protection Act.
- Assist with maintenance of clinical trial documentation.
- Manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines
The Christie Lung Cancer Research Team vision is to build upon our reputation as a local and national leader in clinical trial delivery. Pursuing exemplary care and prioritising the safety and experience of our clinical research participants, carried out by a highly trained and passionate clinical research team.
By becoming a member of the Lung Research Team, you will be joining a dynamic and supportive team who are constantly striving to improve ourselves by work collaboratively across the nursing, medical and administrative teams.
We are a team that strives to develop our staff to the best of their potential and are keen for all members of our team to continue to learn and share knowledge.
I would strongly encourage interested applicants to contact the team to further discuss the roles and how you can become a key member of this exemplary team.
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 core Research and Development team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to trial set up and general trial conduct.
- Set up and initiation of allocated trials within an assigned team, under the guidance of the Senior Clinical Trials Coordinators.
- Track all payments throughout each clinical trial including completion of activity logs and requesting 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.
- Process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines.
- Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements.
- Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas).
- Produce trial workbooks for review by the lead Clinical Research Nurse and Principal Investigator for assigned studies and ensure version control is maintained
- 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.
- Cross check, confirm data and complete query resolution with sponsors and third parties in a timely manner.
- Completion of clinical trial specific databases with data from various sources such as questionnaires, hospital records and other electronic and paper sources.
- 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.
- If required attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team.
- Assist with preparation for audit and inspections within assigned teams.
- Assist with trial document archiving by following the Trust’s 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.
This advert closes on Monday 25 Nov 2024