
LivaNova PLC 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. Our advanced technologies and breakthrough treatments provide meaningful solutions for the benefit of patients, healthcare professionals and healthcare systems.
1001 - 5000 employees
November 19

LivaNova PLC 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. Our advanced technologies and breakthrough treatments provide meaningful solutions for the benefit of patients, healthcare professionals and healthcare systems.
1001 - 5000 employees
• Responsible for creating a clinical evidence generation plan for the therapeutic area(s) and product(s) • Lead cross-functional work streams including clinical study planning • Create business cases, budgets, and clinical protocols for individual studies • Serve as a clinical subject matter expert, advising medical CRB reviewers • Organize and deliver advisory board content and meetings • Support publication of clinical trial results in line with LivaNova strategy.
• Advanced degree (MD, PhD, PharmD) in a healthcare-related field or an equivalent degree • 5-7 years of experience in the healthcare industry • Experience (>5 years) in clinical affairs, medical affairs and/or clinical strategy in the healthcare industry • Leadership and project management experience • Experience in target Therapeutic Area(s) highly desirable • Highly collaborative • Good understanding of marketing, market access, and R&D • Highly competent in study design, analysis, and interpretation of clinical and health economic data.
• 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
Apply NowNovember 19
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