At a Glance
- Tasks: Coordinate follow-ups for a groundbreaking stroke trial and ensure high-quality data collection.
- Company: Join the University of Edinburgh, a leading institution with a vibrant community.
- Benefits: Enjoy flexible working options, generous leave, and a supportive work environment.
- Other info: Be part of a diverse team and enjoy excellent career development opportunities.
- Why this job: Make a real impact in clinical research and contribute to vital health advancements.
- Qualifications: Degree in nursing or relevant science, plus experience in clinical trials and patient assessments.
The predicted salary is between 34610 - 39906 £ per year.
Locations: The Chancellor's Building, Edinburgh, EH16 4SB, GB (100% On-campus)
Organization: Edinburgh University Group
Department: Centre for Clinical Brain Sciences
Apply Before: 06/16/2026, 10:59 PM
Contract Type: Fixed Term
Work Duration: 12 Months
Job Schedule: Full time
Grade: UE06
Number of Openings: 1
Job Function: Academic Support
Grade UE06: £34,610 to £39,906 per annum, pro rata if part time
CMVM / School of Neurological and Cardiovascular Sciences
Full time: 35 hours per week
Fixed term: 12 months (maternity cover)
The Opportunity:
Together we can do great things. Be part of something bigger. With roles from hospitality to research, there’s a career for everyone at the University of Edinburgh. We can offer opportunities for you to develop in your career and make a real difference in the communities around us while contributing to the world at large.
We seek an energetic, organised, motivated Trial Co-ordinator for the LACunar Intervention Trial 3 (LACI-3) funded by NIHR. LACI-3 is the largest and only Phase 3 trial in small vessel (lacunar) stroke in the world. Small vessel stroke is a major cause of vascular cognitive impairment and currently there is no effective treatment.
As the Trial Co-ordinator for the LACI-3 trial, you will be responsible for following up trial participants by phone and post, assessing cognitive function, recurrent stroke and activities of daily living amongst other factors. Your role will be crucial to ensure high-quality, complete and successful data collection for this high-profile trial.
You will work closely with the LACI-3 Chief Investigator, Trial Managers, and implementation teams at the Universities of Edinburgh and Nottingham, the Investigator Group and Site teams. You will also help the Trial Manager and Trial Team with other activities, as appropriate to the stage of LACI-3, such as site set up, organising investigator meetings, maintaining up to date accurate trial records, and preparing various reports on LACI-3’s progress.
You will hold a degree in nursing, a relevant science subject and have experience in clinical trials research. You will have excellent spoken and written communication skills, and data entry skills. You will have experience of conducting patient assessments and interviews by telephone. You will demonstrate flexibility so as to accommodate patient follow-ups in a timely fashion.
You will have up to date knowledge of research ethics and R&D principles, and of Good Clinical Practice with an up-to-date GCP certificate.
A career with us has a range of other benefits that can be tailored to your lifestyle:
- Working within one of the world’s leading universities
- This post is full-time (35 hours per week); however, we may consider part-time or flexible working patterns. The post is primarily office based, but we may consider requests for a mix of office and home (hybrid) working (on a non-contractual basis).
- As a valued member of our team, you can expect an exciting, positive, creative, challenging and rewarding place to work.
- To be part of a diverse and vibrant international community.
- Comprehensive Staff Benefits, including generous annual leave entitlement, a defined benefits pension scheme, a wide range of staff discounts, family-friendly initiatives, and flexible work options.
- Championing equality, diversity, and inclusion.
Prior to any employment commencing with the University, you will be required to evidence your right to work in the UK. Further information is available on our right to work webpages. On this occasion the University will not consider applicants requiring sponsorship for this role. International workers will therefore only be able to take up this role if they can demonstrate an alternative right to work in the UK.
Key Dates to Note:
The closing date for applications is 16 June 2026. Unless stated otherwise the closing time for applications is 11:59pm UK time. If you are applying outside the UK the closing time on our adverts automatically adjusts to your browser's local time zone. Interview dates to be confirmed.
Trial Follow-up Co-ordinator employer: The University of Edinburgh
The University of Edinburgh offers a dynamic and supportive work environment, where you can contribute to groundbreaking research while enjoying a range of benefits tailored to your lifestyle. As a Trial Follow-up Co-ordinator, you'll be part of a diverse international community, with opportunities for professional growth and flexible working arrangements, all within one of the world's leading universities. Join us in making a meaningful impact on health and well-being through innovative clinical trials.
Contact Details:
The University of Edinburgh Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Trial Follow-up Co-ordinator
✨Tip Number 1
Network like a pro! Reach out to people in your field, especially those connected to the University of Edinburgh. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for the interview by practising common questions related to clinical trials and patient assessments. We all know that confidence is key, so rehearse your answers and get comfortable talking about your experience.
✨Tip Number 3
Show your enthusiasm for the role! When you get the chance to speak with the team, let them know why you're excited about the LACI-3 trial and how you can contribute to its success. Passion goes a long way!
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email can leave a lasting impression and shows that you’re genuinely interested in the position. Plus, it’s a great way to reiterate your fit for the role.
We think you need these skills to ace Trial Follow-up Co-ordinator
Some tips for your application 🫡
Show Your Passion:When writing your application, let your enthusiasm for the role shine through! We want to see why you're excited about being a Trial Follow-up Co-ordinator and how you can contribute to the LACI-3 trial.
Tailor Your CV:Make sure your CV is tailored to highlight your relevant experience in clinical trials and patient assessments. We love seeing how your background aligns with what we're looking for, so don’t hold back!
Be Clear and Concise:Keep your application clear and to the point. Use straightforward language and structure your thoughts logically. We appreciate well-organised applications that are easy to read!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way to ensure your application gets to us directly. Plus, you’ll find all the details you need about the role there.
How to prepare for a job interview at The University of Edinburgh
✨Know Your Trial Inside Out
Before the interview, make sure you thoroughly understand the LACunar Intervention Trial 3 (LACI-3). Familiarise yourself with its objectives, significance, and the role of a Trial Co-ordinator. This will not only show your enthusiasm but also help you answer questions confidently.
✨Showcase Your Communication Skills
As a Trial Co-ordinator, you'll need excellent spoken and written communication skills. Prepare examples from your past experiences where you've successfully conducted patient assessments or interviews. Highlight how you adapted your communication style to suit different individuals.
✨Demonstrate Flexibility and Organisation
The role requires flexibility in accommodating patient follow-ups. Be ready to discuss how you've managed multiple tasks or adapted to changing circumstances in previous roles. Use specific examples to illustrate your organisational skills and ability to prioritise effectively.
✨Stay Updated on Research Ethics
Having up-to-date knowledge of research ethics and Good Clinical Practice is crucial. Brush up on these topics before your interview and be prepared to discuss how you’ve applied this knowledge in your previous work. This will show that you're not just qualified, but also committed to maintaining high standards in clinical trials.
