Breast Sonographer - Clinical Trial

Neko Health • New York, NY

3d • $117,000 - $143,000 • Onsite

About The Position

We are looking for an experienced Breast Ultrasound Sonographer to join our clinical team in New York City and perform breast ultrasounds as part of a clinical research study. This role delivers high-quality, independent assessments to research-grade standards. You will perform and interpret breast ultrasound scans for participants enrolled in the study, producing timely results to a standardized electronic case report form. You will work in conjunction with the study's principal investigator to ensure acquisition and reporting meet research-grade quality, working within the study acquisition SOP and Neko's escalation protocols.

Requirements

• ARDMS RDMS certification with the Breast (BR) specialty, or ARRT Breast Sonography certification (ARRT(BS)). These are the two pathways the ACR recognizes for personnel performing breast ultrasound.
• Documented, current breast ultrasound practice, with a minimum of two years' full-time-equivalent breast scanning.
• Independent breast ultrasound scanning and structured reporting experience in an ACR-accredited breast imaging setting or an equivalent quality-assurance framework.
• Strong communication skills, able to explain complex information clearly to study participants.
• Commitment to high clinical standards and active engagement in ongoing professional development.
• Eligible to work in the United States.

Nice To Haves

• Prior ultrasound scanning as part of clinical trials.
• Shear-wave elastography acquisition and reporting.
• Familiarity with the BI-RADS lexicon and structured reporting.
• Experience with Philips ultrasound machines and decision-support software.
• Familiarity with electronic case report form (eCRF) data entry for clinical research.

Responsibilities

• Perform high-quality diagnostic breast ultrasound examinations in line with clinical guidelines and best practice.
• Pass the study-specific acquisition and interpretation qualification task before performing any study scans, with the certificate filed in the investigational site file.
• Independently acquire, interpret, and report breast ultrasound findings, uploading timely results to a standardized electronic case report form.
• Collaborate with the multidisciplinary research team to deliver Neko's clinical trial into breast cancer risk.
• Adhere to the study acquisition SOP consistently.
• Maintain and log equipment QA on-site, liaising directly with the study PI and research team where needed.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed