Clinical Research Assistant

Company Description Cognivus Research Group conducts efficient, high-quality clinical trials across three clinical sites in Western Sydney, Australia. The organization is led by a highly experienced team dedicated to exceptional patient outcomes, rigorous quality of care, and ethical research practices. Cognivus participates in ground-breaking national and international studies, including first-in-human trials, contributing to medical advancement and improved global healthcare. The group places strong emphasis on community engagement and trust-building to support clinical trial recruitment through partnerships with healthcare providers and local organizations. Guided by a vision of empowering healthier futures, Cognivus focuses on patient-centered, scientifically robust clinical research solutions.Role Description The Clinical Research Assistant is a full-time, on-site role based in Wahroonga, NSW. This position supports clinical trial activities by coordinating participant visits, assisting with informed consent processes, and maintaining accurate source documentation and study records. The role involves collecting and processing clinical samples, performing basic laboratory procedures as appropriate, and ensuring adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements. The Clinical Research Assistant will communicate regularly with participants, investigators, and clinical staff, help manage trial logistics and data entry, and assist with safety reporting and follow-up as needed. The role also contributes to continuous quality improvement by supporting audit preparation, monitoring visits, and other site operations that promote efficient and ethical research.Qualifications Candidates should possess strong Interpersonal Skills and Communication abilities to interact effectively with participants, investigators, and multidisciplinary clinical teams.Candidates should possess solid knowledge of Medical Terminology and an understanding of clinical procedures to accurately interpret protocols and document patient data.Candidates should possess Research skills, including data collection, documentation, and basic understanding of clinical trial methodology and GCP principles.Candidates should possess Laboratory Skills relevant to clinical research, such as sample handling, processing, and compliance with safety and infection control standards.Relevant tertiary qualification in health sciences, biomedical science, nursing, or a related field (or equivalent experience) is highly beneficial.Strong attention to detail, organizational skills, and proficiency with electronic data capture systems and standard office software are desirable.Experience in clinical trials, hospital or research settings, and familiarity with ethics and governance processes is an advantage.