Our personal, one-on-one relationships with a large number of top industry CRAs relationships enables us to provide you with the right CRAs for your clinical trials. No matter the Phase or the therapeutic area, we identify the best monitors for your study requirements. Our CRAs are regionally based and have established relationships with clinical research sites to share their knowledge and expertise. Emericlin can adeptly assist with your monitoring and resourcing strategy to identify the best CRA locations to achieve operational and budget efficiency. Whether your need is for a CRA for a short-term Phase 1 study, a CRA team for a longer-term study, or a few CRAs to fill your team, our CRAs report into your Project Management team.
In addition, to our vast monitoring pool of talent, Emericlin can further support US operations for a non-US client by providing a Lead CRA to assist with US operational oversight. We know our staff and we know how they work. Let us work with you to select the most well suited professionals for your studies.
Get in touch with us to learn more about how we can provide CRAs to monitor your studies.
Quality Control Visits, Co-Monitoring, Unblinded Drug Accountability Monitoring, and GCP, vendor, and site audits.
Project Management, Lead CRA services, and clinical study oversight.
Protocol development, Informed Consent documents, and pre-clinical/clinical study reports.