Executive Director, Post-Market Clinical Strategy - Medical Device #0405MM

Our client is seeking an Executive Director, Post-Market Clinical Strategy & Surveillance to lead post-market evidence planning, surveillance strategy, and clinical lifecycle support across a global medical devices portfolio. This role will ensure the organization continues to generate meaningful post-market data, respond to product performance trends, and support regulatory, quality, and business objectives after launch.

This is an excellent opportunity for a senior leader who understands the intersection of post-market clinical evidence, vigilance, risk management, and continuous product improvement.

Key Responsibilities

• Develop and lead post-market clinical evidence and surveillance strategy across commercialized products.
• Partner with Quality, Regulatory, Medical Affairs, and Product teams to assess performance trends and define follow-up evidence needs.
• Guide PMCF, surveillance initiatives, and broader lifecycle evidence planning where applicable.
• Support responses to health authority questions, product changes, and risk management updates.
• Oversee external partners, data review processes, and governance related to post-market evidence activities.
• Build scalable processes for signal review, documentation, and executive reporting.
• Ensure post-market clinical strategy supports both compliance obligations and business decision-making.

• Bachelor’s degree required; advanced degree preferred.
• Extensive experience in medical devices with strong exposure to post-market clinical, surveillance, vigilance, or lifecycle evidence strategy.
• Familiarity with quality systems, regulatory follow-up obligations, and risk management interfaces.
• Strong cross-functional leadership and executive communication skills.
• Experience leading change and maturing post-market capabilities in global organizations.

$225,000 - $280,000 base salary, plus annual bonus and long-term incentive opportunity.

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