Company Overview

Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. We are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.

The Opportunity That Awaits You:

PROCEPT BioRobotics is seeking a passionate and driven Senior Clinical Product Manager to join our growing team. This unique role bridges the gap between clinical development engineering and product management, requiring capability in both areas to play a pivotal role in developing innovative solutions for urological procedures. Are you a highly motivated individual with a deep understanding of surgical robotics and a strong desire to bring impactful products to market? If so, this is the opportunity you've been waiting for. The ideal candidate will have a deep understanding of both clinical workflows and product development processes, along with a passion for leveraging technology to transform healthcare delivery.

What Your Day-To-Day Will Involve:

• Develop and apply in-depth technical and clinical knowledge in urological anatomy, disease states, procedures, and associated products.
• Evaluate clinical publications and data to provide insights to inform product strategy and development and educate commercial partners.
• Partner with Product Managers to clearly define clinical needs and product requirements.
• Collaborate with cross-functional teams including engineering, regulatory, quality, and clinical affairs, providing clinical guidance and support throughout the product development process, such as clinical risks and potential mitigations.
• Develop and maintain relationships with key opinion leaders (KOLs), surgeons, and clinical stakeholders to gather feedback and validate product concepts.
• Lead testing and clinical evaluations for new product concepts and features.
• Drive and execute design, usability, and clinical validation strategies for new products, gaining alignment from key stakeholders.
• Develop and maintain usability risk analyses for current and future products.
• Drive continuous improvement initiatives to enhance product performance, usability, and clinical outcomes based on firsthand case observations, post-market feedback and real-world experience.
• Assist in the development of plans, reports, and other materials to support engagements with the FDA and other regulatory bodies.
• Develop training materials, clinical documentation, and educational resources for internal teams, customers, and users, in partnership with Downstream Marketing and the Global Learning Department.
• Support initial product launches by supporting initial cases during LMR (Limited Market Release).
• Support development and commercial efforts by participating in conferences, symposiums, and customer engagements to showcase product capabilities and clinical evidence.
• Stay abreast of regulatory requirements, standards, and guidelines related to medical devices and surgical robotics to ensure compliance and mitigate risks.

The Qualifications We Need You to Possess

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

• Minimum B.S. in Biomedical Engineering, or a similar discipline.
• Minimum 7 years of experience of clinical development engineering and/or product management in the medical device industry, min of 5 years with an advanced degree.
• Experience driving products and features from concept to launch.
• Demonstrated ability to build strong working relationships with surgeons, surgical staff and internal employees.
• Experience understanding clinical harms and performing clinical risk analysis.
• Knowledge of human anatomy, surgical terminology, and surgical techniques.
• Experience working with surgeons and staff in the operating room.
• Professional work ethic, high capacity, strong analytical and organizational skills, and ability to operate independently.
• Track record of executing complex medical device product development; experience with capital equipment preferred.
• Excellent communication skills and attention to detail.
• Experience working with cross-functional teams.
• Strong multi-tasking skills with an ability to adapt to change.
• Ability to travel up to 30% of the time.
• Computer skills: Microsoft Word, Excel, PowerPoint required, Jama and Jira experience preferred.

The Qualifications We Would Like You to Possess

Medical Device/ Healthcare industry experience is a plus.