Neko is redefining what prevention means, from treating illness when it arrives, to sustaining health before it's ever at risk. Our mission: make data-driven, preventative care accessible to more people, before symptoms appear.
In a single, non-invasive visit under an hour, proprietary technology and direct clinical care combine to deliver personalised, actionable insights. It's a team that thinks in 10x, not 10%. Every role here plays a part in building a world where prevention is the norm, and where your work genuinely helps people live longer, healthier lives.
We’re looking for an experienced Ultrasound sonographer to join our multidisciplinary team in London on a 12 month fixed term contract and help to take ultrasounds as part of a clinical research study.
This is a key role focused on delivering high-quality, independent assessments. You’ll perform and interpret ultrasound scans of adult women who are receiving a breast ultrasound as part of a clinical study. You will work in conjunction with the principal investigator of the study to ensure that assessments and reports are of research-grade quality. This is a fixed term role that lasts for the duration of the study and is based at our clinics in London.
Perform high-quality diagnostic ultrasound examinations in line with clinical guidelines and best practices with focus on breast ultrasound
Pass on the study-specific acquisition and interpretation qualification task before performing study scans, with certificate filed in the investigational site file.
Independently interpret and report ultrasound findings, ensuring timely delivery of results that are uploaded to a standardised electronic case report form.
Collaborate with our multidisciplinary research team to help deliver Neko’s clinical trial focused on better understanding risks of breast cancer.
Adherence to the study acquisition SOP
Equipment QA maintenance logged on-site. Liaise directly with the study PI and research team where needed.
HCPC-registered diagnostic radiographer (or other HCPC-/NMC-registered healthcare professional), holding a CASE-accredited postgraduate qualification in breast ultrasound (PgCert / PgDip / MSc, or a named CASE-accredited breast ultrasound module.
Documented, current breast ultrasound practice, with a minimum of two years’ full-time-equivalent breast scanning.
Advanced radiographic experience of reporting autonomously within the NHS Breast Screening Programme (NHSBSP) or an equivalent quality-assurance framework.
Excellent communication skills, with the ability to explain complex information clearly to study participants.
Commitment to maintaining high clinical standards and engaging in ongoing professional development.
Experience with previous ultrasound scanning as part of clinical trials
Experience with shear-wave elastography acquisition and reporting.
Experience with Philips US machines, and decision support software
Familiarity with data entry as part of clinical research studies.
Monitor clinical trials across therapeutic areas, ensuring site compliance, data quality, and participant safety while coordinating with investigators and project teams and mentoring less experienced associates.
Conduct onsite and remote monitoring, manage site relationships, and take ownership of assigned clinical studies, supporting quality delivery and study performance across therapeutic areas.
Leads scientific safety activities for assigned products across development and post-marketing, driving surveillance, signal evaluation, aggregate assessments, benefit-risk analysis, and regulatory safety support.
Lead clinical trial data management from study design through database lock, ensuring data quality and timelines while overseeing systems, CROs, data reviews, and compliant processes.
Independently manages clinical study activities and supports Study Leads across study execution, vendor oversight, documentation, and compliance with protocols, GCP/ICH guidelines, and company procedures.
