Tewodros Gashu

Clinical Research Coordinator @Liver Center Of Texas, Pllc

Dallas, TX, US

Informed study participants or caregivers about study procedures and outcomes to be expected.• Filled out all source documentation and completed while the study participants visit is occurring and while the study participant is on site for optimal accuracy of data collection.• Completed all source documentation entering EDC within 48 hours of study participants visit.• Attended investigator meetings with principal investigator, asked questions and collected pertinent study information while at investigator meeting.• Attended site initiation visits from various drug sponsors and conduct site initiation tours.• Maintained required records of study activity including case report forms, drug dispensation records.• Communicated with laboratories or investigators regarding laboratory findings.• Performed specific protocol procedures such as interviewing study participants, taking vital signs, performing electrocardiograms (ECG) and collected laboratory specimens.• Draw blood samples for medical testing through venipuncture or capillary puncture.• Experienced in using centrifuges for separating components of a mixture based on density, crucial for sample preparation and analysis.• Recorded adverse events data and confer with investigators regarding the reporting of events to sponsors.• Maintained contact with sponsors to schedule and coordinate site visits/monitoring visits.• Resolved all auto queries in the EDC within 24 hours of query being issued by sponsor.• Dispensed drugs and calculated dosages with drug compliance and provide instructions as necessary to the study participants. • Maintained drug accountability log, new medication shipments and reported to sponsors if lost or damaged. • Initiated and maintained accurate master logs for each study (ICF, patient ID, and enrolments).• Labelled and organized space for all drug received, placed in drug cabinets immediately once the drug arrives to site after being checked in into the drug logs.

Kent State University

Bachelor of Science - BS, Public health with Specializations in Clinical trial research

ATI Career Training Center-Dallas

Diploma, Medical/Clinical Assistant

UT Health San Antonio

Master's degree, Clinical Respiratory

University of Florida College of Medicine

Graduate certificate , Medical Pharmacology and therapeutic