Clinical Program Manager

Sonus Microsystems is reimagining ultrasound for continuous, operator-independent patient monitoring, and we're looking for a Clinical Program 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. You will thrive in this role if you are someone who is hands-on, takes ownership, enjoys solving complex operational challenges, and wants to play a defining role in how Sonus delivers its clinical programs as the company grows. 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 Ensure documentation, approvals and timelines remain aligned throughout execution Identify performance insights and work cross-functionally to implement improvements Partner & Stakeholder Coordination: Serve as the day-to-day operational contact for investigators, clinical sites, KOLs and external partners Travel for key stakeholder meetings within Canada & the US 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: 5+ years of experience 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 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.

The Clinical Program Manager will lead clinical study execution, including site selection, IRB submissions, and day-to-day operational coordination. They will also partner with engineering and regulatory teams to ensure clinical activities align with technical requirements and support FDA/Health Canada submissions.

Candidates must have a strong foundation in clinical trial operations and experience within a regulated medical device environment. Proven ability to manage stakeholders and support regulatory documentation is essential for this role.

• Stock options • Flexibility

• Quality assurancePreferred
• Project managementPreferred

Identified from the job description. Confirm important requirements above.

• Clinical trial operations
• Study start-up
• Site selection
• IRB submissions
• Medical device regulation
• Stakeholder management
• Project management
• Regulatory compliance
• Quality assurance
• Clinical documentation
• KOL engagement
• Milestone reporting
• Risk management
• FDA submission support
• Cross-functional collaboration
• Clinical Documentation
• Influencing Skills
• Influencing Without Authority
• Complex Problem Solving
• Patient Monitoring
• Key Opinion Leader Development
• Stakeholder Coordination
• Medical Devices
• Planning
• Quality Management Systems
• Research
• Artificial Intelligence
• Clinical Practices
• Clinical Trials
• Medical Ultrasonography
• Leadership
• Milestones (Project Management)
• Operations Management
• Operations
• Product Design
• Regulatory Requirements
• Site Selection
• Stakeholder Management
• Timelines
• Enthusiasm
• Institutional Review Board (IRB)

• Healthcare
• Management & Leadership
• Science & Research
• Engineering
• Technology
• Clinical Program Manager
• Clinical Supervisor / Manager
• Health Service Managers
• Medical and Health Services Managers

Minimum experience

5+ years

Posting language

English

Working hours

40 hours per week