Clinical Research Coodinator Date Posted:

11 October 2026

Closing Date:

November 10, 2026

Recruiter:

Sonic Healthcare Location:

Taylor, Texas Salary:

USD72,000

to

USD92,000

Job Type & Industry:

Scientific & Research Contract Type:

Permanent Job Reference:

3016627519-2 Apply for this job now Job Description Sonic Healthcare is seeking a Clinical Research Coordinator in Austin to support diagnostic and clinical studies in a collaborative, patient-centred environment. In this role, you will coordinate daily study operations, including participant recruitment, informed consent, visit scheduling, and data and specimen collection. You will maintain accurate documentation in line with GCP and regulatory standards, partner with investigators, lab teams, and sponsors, and prepare for monitoring visits and audits. This position offers exposure to advanced technologies, global best practices, and strong professional development opportunities. Responsibilities Coordinate day-to-day clinical research activities for diagnostic and pathology studies at Sonic Healthcare's Austin site Screen, enroll, and consent study participants in accordance with study protocols and ethical standards Collect, process, and document clinical data and specimens accurately and on schedule Maintain study source documents, case report forms, and electronic data systems to meet GCP and regulatory requirements Liaise with investigators, clinicians, lab staff, and sponsors to support smooth study execution Schedule study visits, manage logistics, and ensure protocol adherence and visit window compliance Assist with IRB submissions, regulatory binders, and reporting of adverse events Support monitoring visits, audits, and quality checks to ensure data integrity and compliance Educate participants on study procedures and provide high-quality, patient-centered support Contribute to continuous improvement of research processes and adoption of new technologies Required Skills Clinical research coordination Good Clinical Practice (GCP) IRB and regulatory compliance Informed consent processes Clinical data collection and entry Electronic data capture (EDC) systems Specimen handling and processing Study documentation and source management Adverse event reporting Patient recruitment and screening