Trial Monitoring
Trial Monitoring in Mental Health Clinical Trials
MAGNET now offers a Clinical Trial Monitor service to support researchers in delivering high-quality, compliant, and audit-ready clinical trials. Our monitors bring experience, professionalism, and a collaborative approach to every stage of your study.
Key Responsibilities of Our Clinical Trial Monitors:
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Collaborate and Innovate: Partner with project and site teams across all trial phases—from feasibility and start-up through to conduct and close-out—to ensure smooth execution.
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Champion Quality and Integrity: Evaluate and improve site practices, ensure data quality through monitoring and cleaning, and support audit readiness.
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Ensure Regulatory Compliance: Maintain oversight of protocol adherence, investigational product accountability, safety reporting, and regulatory requirements.
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Master Documentation: Support accurate and compliant documentation aligned with ICH GCP standards, including guidance on document generation and maintenance.
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Proactively Monitor Progress: Track study milestones, identify potential risks, and assist with timely implementation of corrective actions when needed.
Whether you need full monitoring support or ad hoc guidance, MAGNET’s Clinical Trial Monitor service is here to help you succeed. Please reach out at magnet@deakin.edu.au
MAGNET also provides guidance on Data Safety Monitoring Board (DSMB) set ups and charters, and a list of volunteers for your DSMB. To access the guidance on DSMBs please click here. If you require members for your DSMB, please email MAGNET at magnet@deakin.edu.au