body {font: normal 400 13px/16px 'Open Sans','Helvetica Neue',Helvetica,Arial,sans-serif;color: #333;margin: 10px;}p,span,div,b,i,u{ line-height: 120%; font-family: 'Open Sans','Helvetica Neue',Helvetica,Arial,sans-serif; } Clinical Research Monitor (CRA) - Medical Device Position Overview We are seeking a detail-oriented Clinical Research Coordinator to oversee and ensure compliance with clinical trials at both site and headquarters levels. This role involves monitoring adherence to protocols, SOPs, GCP, and regulatory requirements. Responsibilities: Oversee clinical trial progress and ensure compliance with protocols and regulations. Develop and maintain relationships with clinical investigators, CROs, hospitals, and research institutions. Review adverse event cases, manage budgets and schedules, and prepare study documents and status reports. Assist in the design, development, and monitoring of clinical evaluation projects. Train investigators and site personnel. Implement clinical development strategies and assist in recommending qualified investigators. Ensure effective recruitment and retention of patients. Requirements: Bachelor's degree or above. Minimum of 2 years of relevant experience Experience in clinical trial management and adherence to GCP and regulatory standards. Hands-on, adaptable, with excellent stakeholder management and communication skills. Prior experience in clinical research is essential. Fluency in Cantonese, Mandarin and English. What you need to do now: Click "APPLY NOW" if you are interested to be part of the team! Alternatively, send your latest CV to [email redacted, apply via Company website] for confidential discussion of your career! All applications applied through our system will be delivered directly to the advertiser and privacy of personal data of the applicant will be ensured with security. Full-time