
1001 - 5000 employees
🏭 Manufacturing
🏥 Healthcare
🧬 Biotechnology
Manufacturing • Healthcare • Biotechnology
LivaNova is a global medical technology company built on nearly five decades of experience and a relentless commitment to improve the lives of patients around the world. With a focus on medical devices, neuromodulation, and cardiac surgery, LivaNova offers advanced technologies and breakthrough treatments that provide meaningful solutions for patients, healthcare professionals, and healthcare systems. Headquartered in London and active in over 100 countries, LivaNova emphasizes bringing both clinical and economic value to its customers, being recognized as a market leader in cardiopulmonary and neuromodulation solutions.
🕒 September 3
🇺🇸 United States – Remote
💵 $160k - $190k / year
⏰ Full Time
🟠 Senior
🏥 Clinical Operations
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👻 Ghost score 11%
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1001 - 5000 employees
🏭 Manufacturing
🏥 Healthcare
🧬 Biotechnology
Manufacturing • Healthcare • Biotechnology
LivaNova is a global medical technology company built on nearly five decades of experience and a relentless commitment to improve the lives of patients around the world. With a focus on medical devices, neuromodulation, and cardiac surgery, LivaNova offers advanced technologies and breakthrough treatments that provide meaningful solutions for patients, healthcare professionals, and healthcare systems. Headquartered in London and active in over 100 countries, LivaNova emphasizes bringing both clinical and economic value to its customers, being recognized as a market leader in cardiopulmonary and neuromodulation solutions.
• Provide overall clinical project management direction, prioritization, and execution of global study objectives on time and within budget • Lead clinical operations teams managing multiple studies aligned with business strategies • Work with study managers, support teams, and monitors to ensure high-quality studies • Provide cross-functional input to development programs and study status updates • Support the Clinical Operations Director in achieving study goals • Oversee program- and study-level outsourcing and take corrective actions on issues • Identify operational gaps and implement optimized clinical operations solutions • Lead strategic initiatives improving efficiency, transparency, quality, and compliance • Apply critical thinking and scientific rigor to clinical study protocol design and review • Manage cross-functional clinical project teams across the clinical portfolio • Ensure studies follow ethical, regulatory, and GCP standards • Assess the assigned study portfolio within 30 days and implement action plans • Identify risks, develop mitigation strategies, and adjust study priorities • Collaborate with Operations, Monitoring, Data Management, Regulatory, Medical Affairs, Clinical Science, and other stakeholders • Manage delivery of multi-center global clinical studies against inclusion rates, timelines, and budgets • Communicate program updates and results to internal and external stakeholders • Assist in developing corporate-wide dashboards • Provide expert input at STC meetings and support clinical strategy and study-related decisions • Advise Product Development teams on clinical considerations for product strategy and lifecycle management • Support long-term clinical strategies for study, publication, and evidence-generation prioritization • Mentor and train project managers and staff in clinical practice, project management methodologies, tools, and procedures • Develop business cases supporting strategic decisions
• Minimum 8 years clinical project/program management experience in a medical device environment with demonstrated consistent professional advancement • Strong project management skills • Ability to convert strategic plans to prioritized product, development and/or operational business objectives • Strong written, verbal, and interpersonal communication skills • A writing sample will be required from top candidates • Ability to troubleshoot and make appropriate decisions under pressure and handle multiple meetings at one time • Exceptional organizational skills • High aptitude for MS Office applications including Outlook, Word, Excel, and PowerPoint • Experience in a fast-paced, complex, dynamic, multi-cultural business environment • Ability to build and maintain effective internal and external relationships • Ability to work independently and in a group environment • Bachelor’s degree in a scientific field or equivalent working experience • Fluent in English • An additional European language is an asset • Regular business travel of 35% or more of the time
• Health benefits – Medical, Dental, Vision • Personal and Vacation Time • Retirement & Savings Plan (401K) • Employee Stock Purchase Plan • Training & Education Assistance • Bonus Referral Program • Service Awards • Employee Recognition Program • Flexible Work Schedules • Discretionary annual bonus
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