Serve as primary coordinator for new study start-up within University systems and with partner hospital sites. Coordinate participant recruitment, informed consent, and specimen collection procedures in accordance with approved protocols, and recommend refinements to the principal investigator. Prepare, submit, and maintain IRB regulatory documentation for assigned studies. Coordinate and monitor timelines for active studies, recommending adjustments to the principal investigator to keep milestones on track. Maintain study databases and protocol files. Order study supplies as needed. Maintain study data collection records in research databases. Track and log biological specimens, maintain specimen records, and coordinate specimen shipments to and from laboratories.pments to and from laboratories. Perform statistical analyses and interpret results in consultation with the principal investigator. Organize study data and prepare manuscripts for publication, including generating tables and figures, editing and formatting, and submitting manuscripts.