Job Description

We encourage you to join us if you have below qualifications: • Full-time presence • Strong communication skills • Good command of Microsoft Office • Planning, problem- solving and teamwork • Being innovative and responsible • Hard-working • Effectively and professionally interacts with Primary Investigators, Research Coordinators, and other site staff to ensure efficient site management throughout the study. • Prepares and conducts site visits as needed • Travels to field sites to ensure site compliance, accurate and complete study management/data collection. • Ensures all site staff are appropriately trained and prepared to conduct the clinical study • Monitor and maintain site staff list, qualification, and training records. • Reviews the quality and integrity of the clinical data • Ensures all reportable events (AEs, SAEs) are identified, clearly documented and reported * Coordinating with Principal Investigator to ensure that clinical research and related activities are performed in accordance with sponsoring agency policies and procedures. * Collaborating to submit regulatory documents to IRB/CTA and register the study at IRCT and any other regulatory submission documents. * Establishing and organizing study files, including study source documentation, informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs. * Entering the data into a database and editing the database records. * Tracking subjects, avoiding lost-to-follow-up * Documenting adverse events