Our Services

Clinical Monitoring / Site Management

Clinical monitoring was the initial "bread and butter" for Trident. We have arguably the most experienced clinical trial team in the industry. Many of our monitors have specific phase 1 monitoring expertise and all have broad therapeutic knowledge.

Our CRAs have a thorough knowledge of local regulations and GCP processes and undergo constant training. Trident has a co-monitoring and training/tutorial program to ensure ongoing quality, consistency and up to date knowledge in our monitoring.

We adapt easily to our customer's needs and requirements with extensive experience in most of the study management and eCRF systems available. We are totally flexible, we can follow your SOPs, our SOPs, or we can do a combination of both - it is up to you.

Our Australian and New Zealand CRAs are based regionally, ensuring easy access to sites for regular contact, prompt issue resolution and cost effectiveness.

Our Indian monitors are ideally based in Mumbai with easy access to key investigator sites. Our CRAs have worked with many of the experienced clinical trial sites within Australia, New Zealand and India and we have a unique and close relationship with the experienced phase I sites, (particularly in Australia).

We can assist you with:

  • Site feasibility and identification
  • Investigator and monitor meeting preparation and set-up
  • All types of monitoring visits including site selection, initiation, routine and study closure visits
  • Local regulatory submissions
  • Obtaining local HREC/EC/IRB approvals
  • Site management
  • Site and client GCP training
  • Monitoring, communication and study plan generation and implementation
  • Query Resolution
  • Blinded and unblinded IP accountability
  • Subject recruitment plans and implementation