Sonus Microsystems is reimagining ultrasound for continuous, operator-independent patient monitoring, and we're looking for a Clinical & Program Operations Manager to join our highly collaborative team of scientists, engineers, and innovators working at the intersection of deep tech and real-world clinical impact. You will contribute to a pivotal stage of the company, where the work you do will help shape the technology, the product, and ultimately the experience of patients and healthcare providers around the world.

Why This Role Matters
This is an opportunity to take ownership of the clinical programs that will help move Sonus' breakthrough Ultrasound AI platform from development into clinical practice. Working directly with the CEO and operations leadership, you will become the operational owner across our clinical studies and clinical programs, ensuring they are thoughtfully planned, effectively coordinated and successfully delivered. As the first dedicated hire in this function, you will have the opportunity to help define how clinical programs operate at Sonus, while remaining deeply involved in the day-to-day execution that drives them forward. You will directly influence product design and functionality to optimize outcomes for both clinical trials and end-user clinicians.

Who We Are
At Sonus, we believe earlier access to diagnostic insight has the power to change and save lives. We are building the next generation of ultrasound technology to help bring advanced medical imaging beyond the traditional walls of healthcare, expanding how and where critical screening and patient monitoring can take place. Built on years of pioneering research, patented polymer MEMS technology, and advanced AI, our proprietary polymer-based Capacitive Micromachined Ultrasound Transducers (polyCMUTs) unlock capabilities not possible with conventional ultrasound systems. We are not just improving existing technology — but helping redefine the parameters of ultrasound and the role it will play in the future of healthcare.

What You Will Do
Clinical Program Leadership





Build robust processes for tracking milestones and deliverables across multiple clinical programs

Identify dependencies, schedule risks and potential delays, proactively resolving or escalating issues before they impact key milestones

Prepare program status updates and milestone reporting for leadership and strategic partners

Clinical Study Execution

Lead feasibility assessments, site selection and KOL engagement to support successful study planning

Prepare, support and submit IRB applications and essential study documentation required for study start-up

Act as clinical coordinator, ensuring documentation, approvals and timelines remain aligned throughout execution

Ensure seamless clinical study execution by identifying performance insights and working cross-functionally to implement rapid, effective improvements

Partner & Stakeholder Coordination

Serve as the day-to-day operational contact for investigators, clinical sites, KOLs and external partners

Partner with engineering, regulatory and quality teams to ensure clinical activities remain aligned with technical and regulatory requirements

Regulatory & Quality Support

Support FDA and Health Canada submissions by compiling, organizing and quality-checking the clinical documentation and study data that feed them, working alongside our regulatory consultants

Maintain clinical documentation in an inspection‑ready state, consistent with our quality system and applicable standards

Ensure clinical activities and records align with design control and regulatory requirements

What You Will Bring

A strong foundation in clinical trial operations across multiple studies or programs, including study start-up, feasibility, site selection, activation,



IRB submissions, clinical documentation and reporting

A background in medical devices, or other regulated healthcare environment, with an understanding of the regulatory and quality requirements that shape clinical studies

Proven stakeholder management capabilities, from internal technical teams through external investigators, KOLs, clinical sites and strategic partners

Experience preparing program status materials and supporting leadership updates

A hands‑on approach, moving confidently between detailed execution and broader program oversight

What Will Set You Apart

History of contributing clinical sections to regulatory submissions (510(k), De Novo, IDE or equivalent)

Experience with milestone reporting for large grants and multi‑stakeholder programs

Sound judgement around priorities, dependencies and risk, with the confidence to surface issues before they become problems

Adaptable and proactive, with a genuine enthusiasm for the dynamic, hands‑on workplace of a growing startup

What’s In It For You
You're joining at a crucial moment in the company's history: before scale, when the decisions you make stick and have lasting impact on the product, the team, and the company we become.

Frontier Technology: Work on a platform with no direct commercial equivalent, alongside the researchers who invented it

Flexibility: High trust, real autonomy, and the flexibility to do your best work

Equity: Meaningful stock options in an early‑stage company with institutional backing

Agency & Impact: Your decisions and innovations will shape the product, not just inform it

We Encourage Diverse Perspectives
We believe that varied backgrounds, experiences, and perspectives help us solve complex problems, and recognize that expertise and potential are not always captured by a job description, so if you can help drive our mission forward, we encourage you to apply!

Please note that we are not able to provide immigration sponsorship at this time.

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📌 Clinical Program Manager (British Columbia)
🏢 Sonus Microsystems
📍 British Columbia