NHSL 228088 Clinical Trials Monitor (LI)
We are looking for an experienced Clinical Trial Monitor to join our dynamic team in ACCORD (Academic Clinical Central Office for Research and Development). The post holder will have responsibility for independently monitoring a portfolio of NHS Lothian/University of Edinburgh sponsored regulated clinical trials across different therapy areas, ensuring these are conducted according to local SOPs and applicable regulatory requirements.
Information and contacts
For further information on the post which is not covered in the job description and person specification please contact Senior Clinical Trial Monitors, Alice Graves and Elizabeth Craig.
Equality and diversity
NHS Scotland is committed to encouraging equality and diversity among our workforce and eliminating unlawful discrimination. The aim is for our workforce to be truly representative and for each employee to feel respected and able to give their best. To this end, NHS Scotland welcomes applications from all sections of society.
Application notice
Please note: we anticipate a high level of interest in this position and may close the vacancy early once a sufficient amount of applications are received. Therefore, please make sure you complete and submit your application at an early stage.
Support for disabled candidates
We will fully support disabled candidates, and candidates with long-term conditions or who are neurodivergent by making reasonable adjustments to our recruitment policy and practices.
Work eligibility
To work in the United Kingdom, there is a legal requirement to demonstrate that you have the relevant permission to work in the country. This permission is granted by the UK Visa and Immigration Service. Further information can be found in the vacancy materials.
PVG and criminal records
This post requires PVG Scheme membership/record. If not currently a PVG member for the required regulatory group, an application will need to be made to Disclosure Scotland before starting. From 1 April 2025, criminal records checks may be updated for regulated roles, with appointment subject to PVG where applicable. Details will be confirmed by the Hiring Manager or Recruitment Team.
Hybrid working
Please note this is a hybrid role (office and home working) with a minimum of 2 days in the office.
Responsibilities
* Independently monitor a portfolio of NHS Lothian/University of Edinburgh sponsored regulated clinical trials across different therapy areas.
* Ensure trials are conducted in accordance with local SOPs and applicable regulatory requirements.
* Collaborate with trial sites and sponsors to manage study milestones, safety reporting, and data quality.
Qualifications
* Experience as a Clinical Trial Monitor or similar role in regulated clinical trials.
Job details
* Seniority level: Mid-Senior level
* Employment type: Full-time
* Job function: Research, Analyst, and Information Technology
* Industry: Hospitals and Health Care
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