Clinical Research Coodinator Date Posted:

11 October 2026

Closing Date:

November 10, 2026

Recruiter:

Sonic Healthcare Location:

Georgetown, Texas Salary:

USD72,000

to

USD92,000

Job Type & Industry:

Scientific & Research Contract Type:

Permanent Job Reference:

3016627344-2 Apply for this job now Job Description Sonic Healthcare in Austin seeks a Clinical Research Coordinator to support high quality clinical trials within a global, medically led diagnostics organisation. In this role, you will coordinate all aspects of study conduct, including participant recruitment and consent, visit scheduling, sample collection and processing, and accurate data entry in compliance with GCP, IRB, and sponsor requirements. You will collaborate closely with investigators, lab and clinical teams, and external partners, helping ensure patient centred, ethical research and contributing to continuous improvement and professional growth in a mission driven environment. Responsibilities Coordinate day-to-day conduct of clinical research studies at Sonic Healthcare's Austin site Screen, recruit, and consent study participants in compliance with protocols and ethics standards Schedule and manage study visits, procedures, and follow-up activities Collect, process, and ship biological samples following GLP/GCP and lab requirements Accurately document data in source records and electronic data capture systems Maintain regulatory binders and essential documents for audits and monitoring visits Liaise with investigators, sponsors, monitors, and interdisciplinary clinical teams Ensure adherence to IRB approvals, safety reporting, and quality standards Support start up, amendment, and close out activities for clinical trials Contribute to continuous improvement of research workflows and patient experience Required Skills Clinical research coordination Patient recruitment and consent Good Clinical Practice (GCP) compliance IRB and regulatory documentation Electronic Data Capture (EDC) systems Sample handling and processing Source documentation and data entry Adverse event reporting Study startup and closeout Stakeholder and sponsor communication