We are a dedicated Clinical Research Associate staffing firm focused on providing you the best CRAs for your trials.
Our 'matchmaking' expertise allow 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're 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 source.
Emericlin looks forward to serving you with the best and brightest in the industry.
Donna Berk, President
Our extensive personal relationships with industry CRAs enable us to provide you with the right CRAs for your study. 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 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 CRA 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 suited professionals for your studies.
We are passionate about the clinical trials industry and may 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
Due to our collective experience, we have developed relationships with many vendors in the industry. If you are interested in other services, we are happy to share our industry experience and make a referral while leaving the assessment and decision making in your control.