Senior Manager, Clinical Trials

At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear implants. We're dedicated to providing outstanding customer experiences through our global audiological care services, ensuring that everyone has the opportunity to engage fully with the world around them.

Guided by a culture of continuous improvement that fosters resilience and self-motivation, our team is united by a shared commitment to excellence and a deep sense of pride in our work, each of us playing a vital role in creating meaningful change.

Here you’ll find a diverse range of opportunities that span both consumer and medical solutions and the freedom to shape your career while making an impact on the lives of others. Join us in our mission to create a more connected world, where every voice is heard and every story matters.

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The Senior Manager, Clinical Trials is the end‑to‑end owner of Advanced Bionics’ late‑phase and pivotal studies, accountable for strategy, protocol authorship, timelines, budget, and regulatory readiness across FDA and EU MDR. As the primary clinical subject matter expert, this role drives clinical program strategy, ensures cross‑functional alignment, and delivers high‑quality evidence for product registration and clinical claims.

• Own the strategic planning, oversight, and accountability for complex, multi-country clinical trials for medical devices in compliance with ICH E6 GCP, ISO 14155, FDA, and EU MDR regulations, within budget and timelines
• Serve as the primary clinical subject matter expert and single study owner — holding full decision-making authority across all trial activities, driving the strategic direction of clinical development programs, and ensuring alignment with business objectives
• Lead and develop key study documents including protocols, ICFs, EDC specifications, statistical analysis plans, and study reports; ensure high-quality data collection, statistical integrity, and timely reporting of results
• Hold accountability for global study delivery by directing Clinical Operations, aligning Clinical Evaluation, Medical Affairs, and the Clinical Development team to ensure consistent, compliant, and strategically aligned execution
• Lead strategic vendor selection and governance globally; oversee vendor performance against study requirements, escalating issues and driving accountability to ensure high-quality deliverables
• Apply project management skills, processes, and tools to plan and execute local, regional, and global clinical trials at Advanced Bionics, including:
  • Scope – Define and approve trial scope; oversee change control processes and hold the cross-functional team accountable to deliverables.
  • Timeline – Develop and manage global enrollment strategy and country allocation; own timelines from start‑up through CSR production and drive contingency plans as needed.
  • Risk – Oversee trial‑level risk identification and escalation; approve the integrated mitigation and contingency plan drawing on scientific, operational, and regional expertise.
  • Budget – Develop, own, and manage global trial budgets; ensure delivery within approved financial parameters and provide strategic financial updates to senior leadership.
• Build and lead a high‑performing team of data managers and scientists; establish data management capabilities, drive evidence generation to support product registration and clinical claims, and lead the build‑out of Global Clinical Trials infrastructure including SOPs, systems, governance, and continuous improvement
• 10–20% travel to conferences and study‑related activities as required.

• Bachelor’s degree in science/clinical/healthcare field, or equivalent combined education
• Advanced degree (MS or equivalent); CCRP, CCRA, or PMP certification a plus
• 8+ years of strong hands‑on experience leading large, complex Phase 3 or pivotal clinical trials in the US and internationally; or equivalent…