At a Glance
- Tasks: Coordinate clinical trials and conduct cognitive assessments for dementia research.
- Company: Join the renowned Dementia Research Centre at UCLH, a leader in innovative healthcare.
- Benefits: Gain hands-on experience in clinical trials with training and support.
- Why this job: Make a real difference in dementia research while developing your skills in a dynamic environment.
- Qualifications: Organised, enthusiastic, and ready to learn about clinical trials.
- Other info: Opportunity for career growth in a world-class research setting.
The predicted salary is between 36000 - 60000 £ per year.
This is an exciting opportunity to be a part of the internationally renowned clinical research team at the Dementia Research Centre (DRC), based within the National Hospital for Neurology & Neurosurgery (NHNN). The Centre has a long history of innovative research in dementia across a wide range of subjects, including longitudinal cohort work, multimodality deep phenotyping of rare dementias, international consortia in genetic dementias and cutting-edge clinical trials in those with and at risk of dementia. The centre is currently involved in first in human studies in Alzheimer’s Disease (AD) using genetic therapies, treatment trials in at risk individuals with genetic AD and with genetic Frontotemporal Dementia (FTD). We are seeking a dynamic, enthusiastic and extremely organized person to provide study coordination and rating to enhance trial conduct at the DRC. The post will provide experience in clinical trials and studies in multiple areas. The successful candidate will be a key member of the clinical research team and will have the opportunity to gain experience in the establishment and implementation of patient-based clinical trials.
Main duties of the job:
- The post will involve administering clinical and cognitive assessments to study participants and their study partners (carer), as appropriate. Post holders will be provided with appropriate training where required ensuring a high level of proficiency in performing cognitive assessments. The post is to start as soon as possible for 1 year in the first instance.
Study coordination:
- Liaising with research participants and clinical trials teams to ensure visits are planned in accordance with study protocols.
- Liaising with multidisciplinary teams to ensure smooth conduct of the study.
- Liaising with service support departments, sponsors and clinical research organisations during set up and running of the trial.
- Ensuring trial activities are invoiced for appropriately; liaising with appropriate finance officers.
Conducting rating scale assessments:
- Conducting cognitive assessments in clinical studies, CDR, ADAS-Cog, RBANS, NPI, RUD-lite, CGIC, etc.
- Working alongside Clinical Research Delivery staff in rating in dementia trials.
Communication:
- Able to communicate with participants and others about trials in appropriate terms.
- Communicate responsively with DRC and Leonard Wolfson Experimental Neurology Centre trials teams.
- Work in the DRC trials team to support the highest standards of trials conduct.
University College London Hospitals NHS Foundation Trust (UCLH) is one of the most complex NHS trusts in the UK, serving a large and diverse population. We provide academically led acute and specialist services, to people from the local area, from throughout the United Kingdom and overseas. Our vision is to deliver top-quality patient care, excellent education, and world-class research. We provide first-class acute and specialist services across eight sites: University College Hospital (incorporating the Elizabeth Garrett Anderson Wing), National Hospital for Neurology and Neurosurgery, Royal National ENT and Eastman Dental Hospitals, University College Hospital Grafton Way Building, Royal London Hospital for Integrated Medicine, University College Hospital Macmillan Cancer Centre, The Hospital for Tropical Diseases, University College Hospital at Westmoreland Street. We are dedicated to the diagnosis and treatment of many complex illnesses. UCLH specialises in women’s health and the treatment of cancer, infection, neurological, gastrointestinal and oral disease. It has world class support services including critical care, imaging, nuclear medicine and pathology. We are committed to sustainability and have pledged to become a carbon net zero health service, embedding sustainable practice throughout UCLH. We have set an ambitious target of net zero for our direct emissions by 2031 and indirect emissions by 2040.
Clinical Trials Coordinator and Rater in London employer: University College London Hospitals
Contact Detail:
University College London Hospitals Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trials Coordinator and Rater in London
✨Tip Number 1
Network like a pro! Reach out to people in the clinical research field, especially those connected to the Dementia Research Centre. Attend relevant events or webinars and don’t be shy about introducing yourself – you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of dementia research and clinical trials. Familiarise yourself with the specific assessments mentioned in the job description, like CDR and ADAS-Cog. This will show that you're not just interested but also knowledgeable about the role.
✨Tip Number 3
Practice your communication skills! Since you'll be liaising with participants and multidisciplinary teams, being able to convey complex information clearly is key. Try role-playing with a friend or family member to get comfortable discussing clinical trials.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team at UCLH and contributing to groundbreaking research in dementia.
We think you need these skills to ace Clinical Trials Coordinator and Rater in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trials Coordinator and Rater role. Highlight any relevant experience in clinical trials, cognitive assessments, or research coordination. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your enthusiasm for the role and the Dementia Research Centre. Share specific examples of your organisational skills and how you’ve successfully communicated with diverse teams in the past.
Showcase Your Communication Skills: Since communication is key in this role, make sure to highlight your ability to liaise with participants and multidisciplinary teams. We love candidates who can convey complex information clearly and effectively, so don’t hold back!
Apply Through Our Website: We encourage you to apply through our website for a smooth application process. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team at the DRC!
How to prepare for a job interview at University College London Hospitals
✨Know Your Trials
Familiarise yourself with the specific clinical trials and studies the Dementia Research Centre is involved in. Understanding the nuances of Alzheimer’s Disease and Frontotemporal Dementia will show your genuine interest and help you engage in meaningful discussions during the interview.
✨Brush Up on Assessments
Make sure you’re well-versed in the cognitive assessments mentioned in the job description, like CDR and ADAS-Cog. Being able to discuss these assessments confidently will demonstrate your readiness for the role and your commitment to high standards in trial conduct.
✨Communication is Key
Practice how you would explain complex trial concepts to participants and their carers. Clear communication is crucial in this role, so think about examples from your past experiences where you successfully communicated difficult information in an understandable way.
✨Show Your Organisational Skills
Prepare to discuss your organisational strategies and how you manage multiple tasks effectively. Given the dynamic nature of clinical trials, showcasing your ability to coordinate with various teams and ensure smooth operations will be a big plus in your interview.