Research Administrator (Data)

The successful applicant will be responsible for the management of all trial data that is generated as part of our clinical trial activity. A lot of the clinical trials we conduct require that data be uploaded to an online electronic platform within a certain timeframe - the post holder will be responsible for ensuring these timeframes are met and that any issues with this process are communicated effectively with the trial sponsors. Part of the data required by clinical trials involve the scan images from CT's/MRI's/PET's - this role will involve requesting and uploading these scans in a timely manner. The post holder will also be responsible for filing all appropriate study documents/materials while working with the nurse team to ensure all records are current and comply with the principles of ALCOA. This post will form a bridge between the consultant/nurse team and the companies we work with so effective and clear communication is vital. This post will also assist in arranging