,As a full service CRO, Grand Pacific CRO’s Clinical Operations team works with you throughout all aspects of your clinical trial to optimise clinical trial design, adopt patient-centric approaches and guide you through global regulatory pathways. We endeavour to be flexible, diligent, and mindful throughout the trial and site management process; constantly looking for innovative approaches to improving subject recruitment and retention, and site productivity.
Our team of experts takes pride in offering the expertise and capabilities you need for the successful development of a new drug or medical device. We successfully deliver access to appropriate sites and patients, developing strategies that will minimise the inherent risks for patient recruitment. From start-up to completion, performance is monitored and measured against contractual timelines, and project costs are tracked to ensure adherence to agreed budgets.