We are currently seeking Clinical Trials Assistant **(** CTA) to join our sponsor-dedicated team in a client facing role. As a vital part of our team, our **Clinical Trials Assistants** **(** CTA) perform daily administrative tasks to support to clinical projects and update clinical systems and databases. This role is a true hybrid position with two days office requirements with our client in North Ryde. You will also perform general administrative tasks as needed. You will have excellent communication, computer, and problem-solving skills, and you will be resourceful, analytical, adaptable, and organised. You will be a natural at building rapport with peers and site staff. When you join IQVIA AUSTRALIA in our sponsor-dedicated team, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. You will be asked to complete a short video screening as part of the interview process. We regret to inform you that we cannot consider sponsorship for this role at this stage so only candidates with full work rights will be contacted. **Essential Functions:** + Prepare, handle, distribute, file, and archive clinical documentation and reports as per the scope of work and standard operating procedures + Review study files periodically for completeness and accuracy + Support CRAs and RSU with the management of Clinical Trial Supplies and tracking information + Track and manage CRFs, queries and clinical data flow efficiently and effectively. + Communicate with the clinical team and provide relevant project information, correspondence and documentation **Qualifications:** + Minimum 6-12 months experience in a CTA role + Flexible and adaptable to different levels of education, training and experience + Updated and maintained clinical documents and systems accurately (e.g., eTMF and CTMS) + Communicated effectively with clients and stakeholders, mastered various computer applications, and resolved complex issues + Familiar with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and ensured compliance in all clinical trials + Completed High or Secondary School diploma/certificate IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes. To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled