Clinical Research Assistant - Research at Icon Group, Chermside

Job Description

Clinical Research Assistant - Research at Icon Group, Chermside Research Brisbane Full Time Research at Icon Group Permanent full-time position, based in our site at Icon Cancer Centre Chermside. Key Points All-round Oncology research role Join Australia’s largest private cancer clinical trials program with access to cutting-edge technology and innovative care solutions. The Opportunity Support our research operations and clinical trials undertaken on-site at cancer treatment centre in Chermside, as part of our nationwide trial programs across Icon Research. All-Round Oncology Research Role : Excellent hands-on cancer treatment research opportunity, with support/training from on-site coordinators, team leads, governance officers, oncologists, pharmacists, oncology nurses and the greater Icon Research community. Career Progression : Clear upskilling, progression and development pathways across Australia’s largest private cancer clinical trials program. Competitive Remuneration , Rewards Programs, Training Programs and Personal Development opportunities. About The Role As a Clinical Research Assistant, you’ll support the coordination and administration of oncology and haematology clinical trials. Reporting to the Research Coordinator Team Leader, your responsibilities include: Key Responsibilities Collect, process and dispatch samples and other materials required by clinical research protocols and prepare and manage clinical trial laboratory kits and samples. Prepare patient visit requirements, assist in appointment scheduling and external hospital liaison for tissue requirements or medical information. Provide support to the research staff in relation to clinical trial administration tasks. Provide support to the investigators conducting clinical trials by ensuring trial documentation is prepared and ready for their review/sign off. Manage investigator site files and essential documents as per GCP. Facilitate the attributable, legible, contemporaneous, original and accurate collection of source data. Work closely with monitors for ongoing monitoring at site and facilitate remote visits. Occasionally travel between our clinics as needed to support the conduct and oversight of cross-clinic research activity. About You We’re looking for someone passionate about clinical research with a keen interest in oncology. Essential Requirements Relevant undergraduate degree (or working towards one) in Health Sciences, Nursing or Allied Health. Excellent written, verbal and interpersonal skills. Proficient in MS office suite and database management. Desirable Experience in Pathology and Laboratory processing will be well regarded. To Apply Please attach a resume and cover letter showing us why you’d love to join us, and what makes you a great fit for the role. Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds. Pre-Employment Vaccination Health Requirement Icon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs). Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs. #J-18808-Ljbffr