Clinical Research Coordinator (Onsite - Aberdeen) At Scottish Brain Sciences we want everyone to enjoy better brain health for life. We are committed to delivering a step change in the detection and treatment of neurodegenerative conditions. To achieve this, w e deliver clinical trials of new tests and medicines that aim to detect brain disease early and treat it before it progresses to dementia. We provide a full-service model for clinical research, with dedicated brain health research centres, an in-house laboratory and imaging services. Together w ith our participants, we are building one of the world’s largest biobanks of genetic, blood and imaging data in neurodegenerative disease. Th ese d ata will speed progress in the search for better Alzheimer’s diagnostics and treatments. We’re looking for a Clinical Research Coordinator to oversee and support clinical studies to support our growing team based at o ur Edinburgh site. This is a high growth, fast paced organisation meaning t he ability to be productive in such an environment is critical. Essential Duties and Responsibilities This is an exciting opportunity to join Scottish Brain Sciences to support a clinical trial from the ground roots. To perform this role successfully, you will have an understanding of compliance and regulatory requirements and ethical standards. The role works closely with investigators, sponsors, vendors, and study participants to facilitate the conduct of clinical trials and research projec ts. I n addition, you will: Ensur e adherence to study protocols and Good Clinical Practice guidelines Assist in recruiting and screening participants for trials Maintain participant visit schedules and book required visits with participants Coordinating and overseeing the running of observational trials and/or CTIMPS Ensu re trials are delivered following regulatory, government, and ethical regulations and requirements Always ensure the safety of participants during their visit to the premises Manage supplies and materials including clinical stocktaking and any products required for clinical use Contribute to the design and delivery of training for trial staff and participants Be the study champion and be able to promote the study internally and externally via meetings, events and seminars Oversee the team that is delivering the clinical research for the project When required, participate in clinical activities such as phlebotomy, ECG and blood pressure recording Quality and Risk, Health, and Safety Management Y ou will be able to identify, assess, manage, and monitor risks within your area of responsibility and c omply with policies, procedures and safe professional practice whilst adhering to relevant legislation, regulations, and standards. You will need to: Understand legal, health and safety standards for the business and ensure standards are met Act as the point of contact for study participants and effectively ensure any questions or concerns are appropriately addressed Ensure the staff rooms and participant lounge is always kept clean and tidy All clinical waste must be removed from the laboratory at the end of the week Clinical waste from clinical rooms must be removed at the end of every day; worksurfaces must be neat and tidy and sanitised at the end of each working week Tasks can be divided among the wider clinical research team Administrative W ork collaboratively with colleagues across Scottish Brain Sciences to ensure adherence t rial protocol is maintained and that professional standards r egarding data are handled appropriately. Collect data and maintain detailed records and database evidence Take ownership for m anaging study documents, protocols and records for participants and trials Support the creation of processes and process improvement within the Company and scope of the project. Work with the wider team to ensure there is adequate cover for continuance of service across this job function Qualifications Bachelor's degree in Nursing, Biology, Health Sciences, or related field At least 1 years’ experience in clinical research coordination or healthcare administration Knowledge of regulatory requirements and clinical trial processes Strong organisational and interpersonal skills Attention to detail and ability to work independently Willingness to learn, adapt and grow with the company This is not an exhaustive list of responsibilities for the role and other duties/tasks may be reasonable requested in accordance with the r ole .