Responsibilities Coordinate daily study operations and participant or patient activities Ensure adherence to protocols, ethics, and GCP standards Maintain study documentation and regulatory records Liaise with investigators, monitors, and teams. Contribute to planning, timelines, and reporting Support audits and inspections. Promote excellence in trial conduct and participant care What You’ll Bring Accountability for quality outcomes and participant well-being. Dedication to excellence and professional standards. Clear, respectful communication. Collaborative mindset and support for colleagues Strong problem‑solving and adaptability. Knowledge of GCP and regulatory frameworks. Background in nursing, science, or related field. #J-18808-Ljbffr
Clinical Study Coordinator
SCIENTIA CLINICAL RESEARCH (SCR)
council of the city of sydney, council of the city of sydney
Published 4 days ago
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