To advance clinical research excellence, the full-time Clinical Research Associate II will manage site engagements, ensure compliance with trial protocols, and drive improvements in data integrity and study performance while working remotely.
Key responsibilities
Serve as the primary point of contact for investigative sites, providing contextual information on clinical trials and fostering strong partnerships Conduct site evaluations, training, and monitoring activities to ensure compliance with regulations and quality standards Develop and implement site engagement strategies, utilizing insights and tools to enhance recruitment and retention efforts Required qualifications Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing) preferred Minimum of 1 year of clinically related experience, including 6 months in clinical research monitoring Advanced knowledge of regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies Strong planning and organizational skills with the ability to manage multiple projects effectively Proficiency in leveraging technology and tools to support site engagement and performance
Experience: 1 year required