We offer a one-year trainee programme for University graduates with life science or relevant background, who do not have clinical research experience to apply for the following entry positions. Trainees with satisfactory performance might continue be employed under a fixed-term contract employment at HKU-CTC.
|Clinical Research Associate||The appointee will participate in setting up study sites, meeting with sponsors and investigators, monitoring clinical studies in accordance with ICH GCP Guidelines and the relevant Standard Operating Procedures (SOPs), and maintenance of study documentation.|
|Project Executive||The appointee will serve as a coordinator to facilitate and monitor study activities, including study contract coordination, study budget preparation and negotiation, ethics submission and study logistic arrangements, from the commencement until the completion of a clinical study.|
|Study Coordinator||The appointee will plan, coordinate and manage healthy volunteer clinical studies and act as the project lead or quality specialist, be the primary liaison between sponsors and investigators, assist in trial volunteer recruitment, perform study procedures and collect data and perform internal quality control of the studies.|
|Data Coordinator||The appointee will provide data management and statistical support including ongoing data management activities, statistical/database programming, statistical planning, analysis and reporting, support the database setup of Electronic Data Capture study.|
|Laboratory Technician||The appointee will assist in plan for the specimen handling workflow for clinical studies, handle specimen such as centrifugation, packaging and shipment and coordinate logistics arrangements on clinical trials among laboratories in the Queen Mary Hospital (QMH).|
|Quality Management Assistant||The appointee will act as the administrator to maintain the Learning Management System, maintain the training curriculum and relevant training assignment documents, update the assigned trackers, manage the archiving of standard quality documents and assist in development of standard quality documents.|