Trial Manager
| Dyddiad hysbysebu: | 20 Awst 2025 |
|---|---|
| Cyflog: | £38,682.00 i £46,580.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £38682.00 - £46580.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 27 Awst 2025 |
| Lleoliad: | Ashton-under-Lyne, OL6 7SR |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9311-25-0589 |
Crynodeb
Monitoring study progress to ensure compliance with and adherence to the project plan and to identify, evaluate and rectify problems. Work with the Chief Investigator to ensure that the Study is meeting its targets, isproducing meaningful output and to predict and plan any changes that warrant requests to changes in protocol, funding or time. Act as the point of contact for the Study across all external and internal agencies. Planning and organising the complex programme across all three national sites managing the various components of the study including site set up, participant recruitment, data gathering and site close down To liaise with relevant funding bodies, research support network (e.g. NIHR Research Design Service) and R&D departments of partner organisations - including principal investigators, finance, study delivery teams and others Planning and supporting the meetings and work of the various groups and bodies associated with the Study. To support the Chief investigator and other team members with relevant research/administrative activities as required Negotiating contracts and collaboration agreements in conjunction with PCFT senior research coordinator and equivalents at other sites Understand the requirements of the various controlling bodies, agencies and frameworks, guiding the project in conforming to those requirements and co-ordinating any necessary audit processes. This will include drafting reports for funders, ethics committees andothers Ensure the inclusion of consumer group representatives at the appropriate levels and times. This will be done in partnership with the service user research associate and service user groups across PCFT To work effectively under time-pressure in order to meet tight deadlines and project milestones To provide advice or demonstrate own research activities or workplace routines To organise their own day-to-day tasks and activities; the post holder must be able to take significant responsibility for planning and implementation of specific elements of the research activities conducted within the project. To be aware of national developments, attend national events and undertake any necessary and relevant training to keep up to date with research developments and related issues as required. Comply with data management and quality assurance according to regulatory guidelines (ICH GCP and Data Protection Act 1998). To comply with departmental policies concerning security, safety and patient confidentiality and to ensure that procedures are carried out with safe systems of work and current legislation. Ensure timely reporting of serious adverse events in line with the UK Policy Framework for Health and social care research Ensure decisions of the trial management committee are implemented in a timely manner Overseeing the tracking of participants through the trial and managing the scheduling of assessments. Overseeing randomisation procedures. Promoting the RELATE-YP trial to staff and service users within the Trust and identifying and approaching potential participants. Undertaking non-clinical baseline research assessments with young people taking part in the trial