Detail oriented Healthcare Professional also trained as Clinical Research Coordinator. Good knowledge and understanding of ICH GCP guidelines, FDA Regulations, Data Management, Informed Consent Process, Clinical Trial Operations from start-up through close-out, ALCOA-C principles for good documentation standard, Monitoring and Query Resolution, Comprehension of Clinical Trial Protocols, Maintaining regulatory binder, DOA, Training logs and other Investigator Site File (ISF) documents. Basic knowledge of patient recruitment, IVRS, EDC, source documents and IP storage. Collecting vitals, blood pressure, weight, pulse, respiration rate of patients. Maintaining communication with patients.
Clinical Research Assistant (New Life Clinical Research)
Chicago, IL