OPIS is seeking a Clinical Research Associate in Australia to manage and monitor multi-site clinical trials, ensuring data quality and patient safety in line with study protocols and ICH-GCP guidelines.
You will perform site feasibility, initiation, monitoring, and close-out visits, while maintaining thorough study documentation and collaborating with sponsors, sites, and project teams.
Clinical Trial Monitoring Specialist employer: OPIS
At OPIS, we pride ourselves on being an excellent employer, offering a competitive salary and a range of benefits that support your professional growth in the dynamic field of clinical data management. Our collaborative and quality-focused work culture fosters innovation and teamwork, allowing you to contribute to international clinical research projects while working alongside highly specialized professionals. Join us in our mission to deliver top-quality trial management and be part of a company that values your expertise and development.
