Vice President of Clinical Operations
1 week ago
Position Overview:
The Mullings Group is seeking a Vice President of Clinical Affairs specializing in heart failure to spearhead the development of their innovative Interatrial shunt integrated with a state-of-the-art remote patient monitoring system.
This organization is dedicated to providing cutting-edge solutions for heart failure management. They have recently secured $33.5 million in Series C funding aimed at enhancing product development and initiating clinical applications of their adjustable interatrial shunt, which features integrated bi-atrial pressure monitoring capabilities.
The device is designed with a flow channel that can be adjusted post-implantation, utilizing a proprietary induction catheter to modify its geometry. Furthermore, the implantable system is equipped with sensors that continuously capture pressure readings from both the left and right atria multiple times daily, requiring no patient interaction.
These frequent measurements offer healthcare providers a comprehensive view of a patient's hemodynamic condition, facilitating improved management of shunt therapy and informed medical decisions. Heart failure is a progressive ailment affecting approximately 6.5 million individuals in the United States and around 26 million worldwide.
Key Responsibilities:
- Lead executive-level initiatives in clinical affairs, with a preference for experience in regulatory affairs or quality assurance.
- Oversee first-in-human trials and larger studies for regulatory approval in the US and/or EU, with a strong emphasis on leadership throughout all trial phases.
- Possess extensive cardiovascular experience at a senior level, particularly in heart failure, with a preference for interventional cardiology expertise.
- Demonstrate a solid background in medical devices.
- Exhibit exceptional interpersonal skills and the ability to engage effectively with global medical key opinion leaders.
- Be open to travel for conferences and case studies, including international destinations.
- Have experience with class III implantable devices or complex class II products.
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