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Project Management and Site Monitoring

Avance Clinical is a recognised Australian CRO for delivering high-quality research outcomes through the highest levels of customer service.

The company provides each clinical research trial with a dedicated project manager to ensure that milestones are reached, timelines are met and that our clients receive effective communication and ongoing status reports.

From the first conversation to the delivery of the final report, our clients are fully informed throughout the process; irrespective of project complexity.

Our project managers and monitors are involved in all aspects of clinical trial management, including:

  • Feasibility assessments
  • Study design
  • Protocol review
  • Development of patient information and consent forms
  • Ethics Committee submissions
  • Review of eCRF design and development
  • Investigator selection / facilitating investigator meetings
  • Site selection
  • Pre-study visits
  • Site Initiation visits
  • Interim Monitoring visits
  • Close-out visits

Avance’s clinical research associates are fully trained to appreciate the complexity of each specific clinical research trial and ensure that monitoring is conducted to the highest standard.

All trials are monitored in accordance with Australian regulatory requirements and ICH GCP. To ensure the seamless exchange of information each clinical research trial is assigned a project manager as a single point of contact.

Avance has staff experienced across all phases of clinical trials and collaboratively supports the Australian CRO arm of multinational trials.

The company’s quality assurance department audits and reports on the monitoring, collection and reporting of accurate, precise, and valid data.

Avance has an extensive suite of standard operating procedures to conduct clinical research trial activities. additionally, Avance can adapt seamlessly to your sop and requirements if desired.

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