Clinical Research Coordinator / Cognitive Rater

The Imperial Memory Unit (IMU) has been running clinical trials for over 13 years, focusing on disease modifying treatment trials in early Alzheimer's disease but also including observational studies and trials of advanced diagnostics. The Imperial Memory Unit was recently awarded funds by the UK Dementia Trials Network (UKDTN) to support the delivery of early phase clinical trials in Alzheimer's disease. This post is funded by the aforementioned. Responsibilities for this post will include collection of research data (including cognitive data), and coordination of patients participating in clinical research. Therefore, the post holder must have prior experience of administering cognitive and neuropsychological rating scales in Clinical Trials of Investigational Medicinal Products (CTIMPs) in Alzheimer's disease or other dementias. Research coordination experience in the aforementioned field is desirable. The post holder will also be expected to develop skills and knowledge relating to the conduct of clinical research. The majority of time will be spent in a hospital research clinic setting (namely Hammersmith hospital (main site) and Charing Cross hospital) during patient visits and will also spent time facilitating recruitment by calling patients, and if necessary visiting other West London Memory Clinics. The post holder will facilitate high standards of care and work closely with the staff of the clinical dementia service.,

• Is accountable for the timely and accurate documentation of trial data according to ICH Good Clinical Practice and EU directive on clinical trials. (The directive ensures all clinical trials are conducted to a high legally binding standard).
• Functions within a collaborative practice role with the multidisciplinary team (MDT) to provide expertise in the assessment, planning, implementation and evaluation of clinical research protocols.
• Demonstrates an excellent understanding of different cognitive scales (e.g. CDR, ADAS-Cog, RBANS) and their use in Clinical Trials of Investigational Medicinal Products (CTIMPs) in Alzheimer's disease and other dementias.
• Demonstrates autonomy as well as the ability to collaborate within the MDT.
• Required to use own initiative, take responsibility for decision-making and prioritise own workload within a team and individual context
• Continued in Job description
  
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