The Clinical Trials Assistant (CTA) is a multi-skilled position that supports research nurses and coordinators within a team, or several teams, and is a key administrative liaison and support for several projects. This position will mainly support our Canadian Cancer Trials Group (CCTG) and our Radiation Therapy Oncology Group (RTOG). Responsibilities include helping to organize and complete various regulatory tasks associated with the initiation or maintenance of clinical trials conducted under Good Clinical Practices, as well as data entry completion for patient follow-up and survival. They help set up study patient and monitoring visits, appointment bookings, organize study & lab supplies and ensure the completeness or delivery of relevant documentation. The incumbent must demonstrate the ability to recognize and maintain confidential information, have highly developed organizational skills, and keen attention to detail. They will also multi-task effectively in a busy area with multiple interruptions and competing demands, and have good problem solving and communication skills. They can work cooperatively and professionally with clinical trials staff and physicians. Lastly they are able to function both independently and as a team member in a fast paced, dynamic office environment.