Director, Clinical Affairs

Kardium Inc.

15h • Hybrid

About The Position

By joining the Kardium team, you can help make a difference in the lives of millions around the world. We have developed a ground-breaking medical device for the diagnosis and treatment of the most common heart rhythm disorder, atrial fibrillation – which can cause stroke, heart failure, and other heart-related complications.
Kardium’s mission is to deliver the best treatment for atrial fibrillation. To achieve this, we have developed The Globe® Pulsed Field System – a revolutionary solution designed by our world-class technical team. The Globe System offers strong, unique, and customer-valued advantages over other treatments on the market, and leading physicians are already using it and helping to share our story.
We have obtained FDA approval and officially begun the commercial launch of the Globe® Pulsed Field System. This is a pivotal and exciting time in our journey, as we bring this life-changing technology to patients!
We are seeking a Director, Clinical Affairs who will lead the planning, execution, and oversight of global clinical studies focused on our electrophysiology and catheter ablation portfolio. This role requires deep domain expertise in cardiac electrophysiology, particularly in the design and execution of catheter ablation clinical trials. You’ll collaborate with cross-functional teams, regulatory bodies, and key opinion leaders (KOLs) to ensure clinical programs align with product strategy and regulatory pathways.
Please note, this opportunity is a hybrid work arrangement, located in Burnaby, BC.

Requirements

• Advanced degree (MD, PhD, or equivalent) preferred; Master's in a related field with extensive experience will be considered.
• Minimum 8–10 years of clinical affairs experience in the medical device industry, with a strong emphasis on electrophysiology and catheter ablation.
• Demonstrated leadership in planning and executing complex, multi-center clinical trials.
• Proven track record of successful regulatory interactions and submissions (FDA, EMA, etc.).
• Deep understanding of electrophysiology clinical workflows, unmet needs, and physician decision-making.
• Exceptional communication, leadership, and cross-functional collaboration skills.
• Willingness to travel domestically and internationally (up to 20%).

Nice To Haves

• Clinical background in cardiology or electrophysiology preferred (e.g., former EP clinician or clinical specialist).

Responsibilities

• Lead the strategic design and execution of clinical studies (feasibility, pivotal, post-market) for catheter ablation devices and therapies.
• Serve as the clinical subject matter expert for electrophysiology, ensuring scientific rigor and clinical relevance across all programs.
• Collaborate with R&D, regulatory, marketing, and medical affairs teams to align clinical objectives with business goals.
• Develop relationships with global KOLs, investigators, and institutions to support study recruitment and protocol development.
• Oversee CROs, clinical sites, and internal teams to ensure adherence to timelines, budgets, and regulatory compliance (GCP, FDA, EU MDR).
• Support regulatory submissions (IDE, PMA, CE Mark) and interface with regulatory agencies as needed.
• Analyze clinical data and provide strategic input on interpretation, reporting, and publication efforts.

Benefits

• Total cash – the total cash we’ve listed for this position includes a base salary, plus a contribution to a Registered Retirement Savings plans (RRSP) to help support your financial goals.
• Comprehensive medical & dental coverage – for all permanent employees – effective as of Day 1, with no waiting period.
• Work-day flexibility – additionally, we provide 3 personal days per year.
• Support – for you (and your dependents) overall well-being.
• Career progression and learning support.
• Professional membership support.

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Education Level: Ph.D. or professional degree