Clinical Research Assistant
Houston, TX 77001
Records, interviews, questionnaires, diagnostics and other sources.
Awarded two-year contract by Genentech Pharmaceutical out of 100 clinical research coordinators to conduct monthly teleconferences
Perform regulatory and quality assurance audits on industry sponsored, and Investigator initiated protocols at site and submit findings and recommendations in writing.
Liaison between Sponsor appointed contacts and Principal Investigators at site.
Obtain blood samples, cultures, and other specimens for laboratory documentation.
Accurately collect and record all necessary data during study visit.
Ensure prompt and accurate reporting of adverse events and con med changes to sponsor and IRB's.
Promptly request all necessary medical records for SAE reporting report to the sponsor and IRB within required timeframe.
Maintain all study binders and ensure that all required regulatory documents are updated in the site's regulatory binder throughout the life of the study.
Resolve sponsor queries in electronic data capture and sponsor specific case report forms.
Must have a Bachelors or Ophthalmology Tech experience required.