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Kardion

Heart pump medical device company

Executive Assistant

Full-Time
$125k - $145k/yr+ Equity + Annual incentive bonus
Senior
Bachelor's
Irvine, CA, USA
In PersonOn-site in Irvine, with occasional early-morning calls with Germany and occasional travel to Stuttgart.
Administrative & Executive AssistanceExecutive Support

About the job

Requirements
  • At least 7 years of executive assistant experience, including supporting a CEO or other C-suite executive and supporting several executives at once.
  • Advanced PowerPoint skills and a strong eye for clear, well-designed slides.
  • Excellent calendar management and prioritization skills, including across time zones.
  • Sound judgment about what to handle and what to escalate, and comfort pushing back politely on senior leaders.
  • Experience planning meetings and events from start to finish, including venues, vendors, and budgets.
  • Strong project coordination skills, including tracking many moving pieces and following through.
  • Clear, professional written communication.
  • Proven discretion with confidential information.
  • Advanced Microsoft 365 skills, including Outlook, Teams, Word, and Excel; experience with DocuSign and expense tools.
  • Comfort working in a fast-paced startup with changing priorities.
  • Occasional early-morning calls with Germany and after-hours needs.
  • Excellent verbal and written communication skills in English, with the ability to communicate clearly and professionally with colleagues in the US and Germany.
  • The employee is regularly required to sit, stand, walk, talk, and hear for up to 8 hours per day; regularly lift and carry up to 10 pounds and occasionally up to 20 pounds; and use a keyboard and computer daily and perform close-vision tasks.
Responsibilities
  • Manage calendars and scheduling for the CEO and executive team across U.S. and German time zones, including early-morning calls with the Stuttgart team.
  • Act as the team's shared point of contact for scheduling and meeting logistics, balance competing requests fairly, and take conflicts to the CEO.
  • Protect time for leaders' most important work, and prepare agendas and materials ahead of meetings.
  • Build, format, and proofread PowerPoint presentations for the CEO and executive team, turning rough notes and data into clear, polished slides.
  • Coordinate executive team meetings, monthly reviews, quarterly planning sessions, and offsites by scheduling them, drafting agendas for the CEO's review, gathering materials from presenters, taking notes, and tracking action items to completion.
  • Plan all-hands meetings and leadership events from start to finish, including offsites and leadership dinners, handling venues, vendors, budgets, invitations, and day-of logistics.
  • Support projects for the CEO and executive team by tracking deliverables, deadlines, and status, and keeping people on schedule.
  • Schedule investor, partner, and visitor meetings, and coordinate guest visits to the Irvine office.
  • Arrange domestic and international travel for the executive team and process expenses accurately and on time.
  • Route documents for signature for Kardion, Inc. and Kardion GmbH with Finance and Legal.
  • Handle sensitive and confidential information with discretion.
  • Perform other duties as assigned.
Desired Qualifications
  • Medical device, life sciences, or healthcare experience.
  • Experience at a venture- or private equity-backed company.
  • German language skills or experience working with European teams.

About the company

Kardion is a medical technology company developing a catheter-based heart-support system. The company researches, engineers, tests, and prepares clinical and manufacturing programs for an implantable cardiovascular device. It serves clinicians, patients, researchers, regulators, clinical partners, and medical-device suppliers. Its operating model centers on device development coordinated across engineering, clinical, quality, regulatory, and manufacturing teams. Teams work across biomedical engineering, clinical affairs, quality, regulatory, manufacturing, research, and operations. Its work connects cardiovascular medical devices expertise with coordinated delivery for clinical and healthcare stakeholders.

Company Size

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Company Stage

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Total Funding

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Headquarters

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Founded

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Simplify Jobs

Simplify's Take

What believers are saying

  • PICANTE enrolled in 2026 across Hartford and Christ Hospital, proving active clinical execution.
  • September 2026 trial pages describe an enrolling pivotal study, not a stalled prototype.
  • Patents published in March and August 2026 strengthen bargaining power with partners and acquirers.

What critics are saying

  • PICANTE results are due December 31, 2026; a miss blocks FDA and hospital adoption.
  • Kardion shows no disclosed funding, limiting manufacturing scale and trial expansion.
  • Impella’s incumbent network at Abiomed and Johnson & Johnson crushes weak clinical superiority claims.

What makes Kardion unique

  • Kardion’s CORY P4 targets high-risk PCI with randomized head-to-head evidence against Impella CP.
  • The company owns implantable vascular support patents filed in 2026, including flow-monitoring designs.
  • Steve Williamson became CEO in August 2026, signaling a commercialization-focused MedTech team.

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Benefits

  • Health Insurance
  • Dental Insurance
  • Vision Insurance

Company News

PR Newswire
Sep 22nd, 2026
Cadence Neuroscience appoints medtech executive Chris Cronin as CEO to lead clinical execution and platform growth.

Cadence Neuroscience appoints medtech executive Chris Cronin as CEO to lead clinical execution and platform growth. Cadence Neuroscience Sep 22, 2026, 09:00 ET Veteran medtech executive brings leadership experience across neuromodulation, clinical-stage company building, and commercialization; Founder Kent Leyde to lead technology and product development as CTO REDMOND, Wash., Sept. 22, 2026 /PRNewswire-PRWeb/ - Cadence Neuroscience, a clinical-stage company developing a biomarker-guided platform for personalized neuromodulation, announced the appointment of medtech executive Chris Cronin as Chief Executive Officer. Cronin joins as Cadence prepares for clinical evaluation of its investigational Biomarker Targeted Stimulation (BTS) system in focal drug-resistant epilepsy as its first indication, while building the capabilities to develop the platform across additional neurological conditions. Cronin brings nearly three decades of experience across medical technology, healthcare, finance, business development, and commercialization, including leadership experience in neuromodulation and other complex therapeutic-device categories. Kent Leyde, company founder, will become Chief Technology Officer and continue to lead Cadence's technology development, product strategy, and key external collaborations. Cronin most recently served as CEO and President of KARDION, a cardiovascular medical technology company, where he led the organization through a critical stage of growth as it moved from first-in-human to pivotal study. Previously, he held executive leadership roles at MOBĒ, helping scale the early-stage healthcare company, and spent more than a decade at Medtronic in leadership roles spanning cardiac and restorative therapies. As a Business Director at Medtronic, he held P&L responsibility across eight countries and regions for one of the company's largest franchises, with experience spanning neuromodulation modalities including deep brain stimulation, spinal cord stimulation, and intrathecal baclofen. Cadence's investigational BTS system is designed to use patient-specific neural biomarkers to inform stimulation and measure the brain's response to therapy. This biomarker-guided approach is intended to provide clinicians and researchers with real-time physiological feedback that may support more personalized and adaptable neuromodulation. Cadence is initially evaluating BTS in focal drug-resistant epilepsy, a serious condition in which many patients continue to experience seizures despite available anti-seizure medications and may have limited treatment options. This substantial unmet need makes focal drug-resistant epilepsy an important first indication for clinical evaluation of Cadence's platform. "Cadence has developed a fundamentally different approach to personalized neuromodulation - using patient-specific biomarkers not only to guide stimulation, but to measure how the brain responds," said Cronin. "The company has built a compelling technical and scientific foundation, and I'm excited to work with Kent, the board, clinical collaborators, and the broader team at this pivotal stage as we prepare for an important clinical study in focal drug-resistant epilepsy and build toward the broader potential of the Cadence platform across neurological conditions." "Chris' patient-centered approach to healthcare and medical devices is closely aligned with the way we've built Cadence from the beginning," said Leyde. "He brings deep business and medtech leadership experience at an important point in our growth. I'm pleased to have Chris leading the company while I focus on developing the technology and products at the heart of our work." "Cadence has reached an important inflection point," said Dan Moore, Independent Board Director at Cadence Neuroscience. "The company combines innovative technology with a clear initial clinical focus. Chris's experience in complex therapeutic-device categories and growth-stage medtech leadership complements Kent's continued technical leadership, positioning Cadence to execute its clinical plan and build toward future commercialization." Cadence's technology originated from research conducted by a Mayo Clinic Neurology and Neurosurgery team led by Gregory Worrell, M.D., Ph.D., a Mayo Clinic epileptologist and lead investigator. Cadence is building on this scientific foundation as it advances the BTS system through clinical evaluation. About Cadence Neuroscience Cadence Neuroscience is a clinical-stage medical technology company developing a biomarker-guided platform for personalized neuromodulation. Its investigational Biomarker Targeted Stimulation (BTS) system is designed to use patient-specific neural biomarkers to inform stimulation and measure the brain's response to therapy in real time. Cadence is initially advancing BTS in focal drug-resistant epilepsy, with a long-term goal of developing the platform for additional neurological conditions. Founded in 2017 and headquartered in Redmond, Washington, Cadence is building on technology originating from Mayo Clinic research. Cadence is backed by leading healthcare and technology investors, including F-Prime Capital, Jazz Venture Partners, LivaNova, Angelini Lumira Biosciences Fund, and Mayo Clinic. For more information, visit cadenceneuro.com. Mayo Clinic and Dr. Worrell have a financial interest in the technology referenced in this news release. Mayo Clinic will use any revenue it receives to support its not-for-profit mission in patient care, education, and research. Cadence Neuroscience is developing investigational medical technologies that have not been approved or cleared by the U.S. Food and Drug Administration (FDA) or other health authorities. Any forward-looking statements reflect current expectations and are subject to risks and uncertainties. Actual results may differ materially. This information is for educational purposes only and does not constitute medical advice or investigational device promotion. Patients should consult qualified healthcare providers regarding diagnosis and treatment options. Currently, these investigational technologies are only accessible through participation in a clinical trial. To learn more about these investigational technologies and how to access them, talk with your qualified healthcare provider or visit www.clinicaltrials.gov. Media Contact Alysa Wood, Cadence Neuroscience, 1 (425) 298-3184, [email protected], https://cadenceneuro.com/ SOURCE Cadence Neuroscience