Amarex Clinical Research, LLC
Sarah E. Garrett has extensive experience in clinical data management, currently serving as Clinical Data Manager II at Amarex Clinical Research, LLC since February 2016. Previously, Sarah worked in various roles at Amarex, including Clinical Data Associate and Clinical Data Coordinator. Prior to joining Amarex, Sarah served as a clinician at Secure Medical Care from July 2013 to April 2016 and at Physicians Treatment Center from April 2004 to May 2013. Sarah holds a Bachelor of Science degree in Biomedical Sciences from Jefferson College of Health Sciences, earned between 2008 and 2011.
Amarex Clinical Research, LLC
Amarex is a global, full-service Contract Research Organization (CRO), whose leadership team has significant expertise conducting biomedical research, and whose combined experience includes the design and conduct of several hundred clinical research projects in many therapeutic indications. Amarex provides comprehensive services in Project Management (Phase I-IV, BE/BA, PK/PD), Regulatory Affairs (FDA Applications and meetings, Applications to International Health Authorities, GxP Compliance Audits), Clinical Operations, Adaptive Study Designs, Statistical Analysis, Data Management, Medical Monitoring, Safety and Pharmacovigilance, and General Consulting. Amarex can take your product through the entire approval process, from creating the regulatory approval strategy, to conducting trials, to writing the marketing approval application. Join our growing list of clients with approved products. Amarex provides high quality and cost efficient services. Sign-up to receive invites to webinars, training courses and the latest cutting-edge information on clinical trials: https://go.pardot.com/l/129231/2020-07-27/39ng9k