We are a dedicated Clinical Research Associate staffing firm focused on providing you the best CRAs for your trials.
Our 'matchmaking' expertise allows us to provide you with the experienced staff you want. We are a hands-on management team that strives to match your business needs with the CRA's that best suit your project, budget requirements, timelines, and individual personalities. We are proud to share over 20 years of experience providing pharmaceutical, biotech, and device companies with exceptional clinical research staff that excel in protocol knowledge and effective site management. Whether it is assembling a team of CRAs for a specific study or identifying a single CRA to complement your existing team, we are your expert source.
Emericlin looks forward to serving you with the best and brightest in the industry.
Donna Berk, President
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! We know how they work! Let us work with you to select the most well suited professionals for your studies.
We are passionate about the clinical trials industry and can also support your clinical trial needs with:
Quality Control Visits, Co-Monitoring and Unblinded Drug Accountability Monitoring
CLINICAL STUDY MANAGEMENT
Project Management and Lead CRA services
Clinical study protocol, Informed Consent, pre-clinical and Clinical Study Reports
GCP, vendor and site audits