Clinical Research Assistant
The Woodlands, Texas, United States
Prepare visit-specific documentation and charts for Clinical Research CoordinatorCoordinate and schedule patient visits within patient/study-specific windows per protocol guidelinesInform patients and obtain written consent in regard to ICF’sMonitor patient flow for CRC and assist in patient care and managementAccurately collect and record all necessary data (e.g. demographics, medical history, adverse events, concomitant medications, etc.) during study visit to later transcribe from the source document to the Electronic Case Reports FormsAdminister all mandatory questionnaires to study subjectsSet up, prepare patients for and conduct electrocardiogramsScribe ocular exams for doctors and confirm appropriate treatment per protocolPromptly request all necessary medical records for Serious Adverse Event reportingCollection, processing and shipment of laboratory specimens for analysisPerform intraocular pressure checks post-injectionsReview and resolve data management queries as needed