NEURALIEVE, INCClinical Research Associate
Nov. 2007 - Jun. 2009Created training programs to educate patients and sites on the study and device.
Responsible for study management activities including but not limited to: manage the data management vendors including contracts, timelines, reports and daily activities and IRB submissions. Responsible for the writing and releasing of SOP's. Site monitoring includes but is not limited to: maintain regular contact with sites, assist sites with protocol, case report form completion, IRB submissions, site contracts, and ensure queries are quickly resolved. Responsible for routine clinical coordinator duties including but not limited to: development and tracking filing systems for regulatory documents, site contact information, and case report forms (CRF's) as well as preparation of study boxes, mass mailings and other correspondence. Responsible for phone and email communications with company, hospital, and contract research organization staff as well as other tasks as needed to support the Clinical Department.