Edwards Lifesciences Corp

Edwards Lifesciences is the global leader in the science of heart valves and hemodynamic monitoring. Driven by a passion to help patients, the company partners with clinicians to develop innovative technologies in the areas of structural heart disease and critical care monitoring that enable them to save and enhance lives.

We partner with physicians to innovate products designed to help patients live longer, healthier and more productive lives. We focus on medical technologies that address large and growing patient populations in which there are significant unmet clinical needs.

Edwards Lifesciences Corp Remote * (Irvine, CA, USA)
Feb 24, 2021
This is an exciting opportunity for an exceptional Scientific Communications professional with significant publication experience to join a team that is boldly designing transcatheter mitral and tricuspid therapies from the ground up. Edwards TMTT division is dedicated to solving the complex challenges of mitral and tricuspid disease in order to transform treatment and significantly improve patients' lives. The Manager, Scientific Communications will lead the design and implementation of scientific communication activities. Key Responsibilities: Proactively prioritize, identify, assess, and critically summarize relevant scientific and medical literature across therapeutic area. Synthesize, assess, and communicate potential impact of key findings to internal stakeholders. Interpret study results and collaborate with HCPs (e.g., study Investigators, physician) in the development of scientific communications content, such as conference proceedings (e.g., abstracts and...
Edwards Lifesciences Corp Remote * (Irvine, CA, USA)
Feb 22, 2021
Edwards has an exciting opportunity in the Transcatheter Heart Valve (THV) group, focused on developing minimally invasive solutions for patients suffering from structural heart disease. As the Senior Manager, Clinical Project Management, you will lead a cross-functional project team to plan, execute, and achieve clinical trial objectives within the Sustaining and Indication Expansion Clinical Programs and New Product Development portfolios. Key Responsibilities : Planning: Develop and manage clinical project plans to identify and complete clinical trial milestones with accountability for successful completion of all project deliverables for high-profile, significant, and more complex clinical trials according to GCP, all applicable regulations and SOPs. Serve as the primary lead of assigned clinical trial(s). Oversee selection of clinical vendors and study sites and preparation of clinical portions of IDE and PMA submissions. Leadership and Accountability: Responsible for...
Edwards Lifesciences Corp Remote * (Atlanta, GA, USA)
Feb 21, 2021
This is an exciting opportunity for you to join a team boldly designing transcatheter mitral and tricuspid therapies from the ground up. Edwards' Transcatheter Mitral and Tricuspid Therapies team is deeply dedicated to solving the complex challenges of mitral and tricuspid disease in order to transform treatment and significantly improve patients' lives around the world. The Senior Specialist, Clinical Research Associate - Remote will ensure clinical trials are conducted and reported in accordance with all applicable regulatory requirements with a responsibility of field site co-monitoring of up to 50%. Essential Job Functions/Key Responsibilities: Responsible for study start-up and study conduct activities including drafting ICF study specific template and TMF plan, approving study specific essential documents list, managing sites. Communicating the status of study progress and co-monitoring activities. Partner with cross-functional team (e.g., clinical data management,...
Edwards Lifesciences Corp Remote * (Irvine, CA, USA)
Feb 20, 2021
Edwards' Critical Care technologies improve the lives of millions of patients each year. Through continuing collaboration with our clinicians, ongoing education, and our never-ending quest for innovation, Edwards continues to develop innovative hemodynamic management solutions that enable clinicians to provide better care to patients in the OR, ICU, and ED settings. The Medical Writer will be responsible for developing accurate and effective Clinical, Scientific, and Regulatory documents and presentations for external scientific conferences and meetings. Key Responsibilities: Research, create, and edit moderately complex scientific documents and presentations of clinical research based on input from the Clinical Team, Key Opinion Leaders (KOLs), and physician investigators Write moderately complex clinical documents for regional regulatory submissions, including but not limited to: briefing documents, previous human experience summaries, investigator brochures, study protocols,...