Jobid: 3195971478 (0.11)
Overview
In this role you drive the AV&I clinical evidence strategy across the full product lifecycle to demonstrate clinical value, support regulatory success, and improve patient outcomes. You’ll work with cross-functional teams to embed evidence plans into roadmaps, lead global clinical studies and publications, and shape external communications with regulators and partners. You will build and mentor a Clinical Affairs team. This is a unique opportunity to influence how advanced visualization and informatics technologies translate into meaningful clinical impact at scale.
Arbeidsvoorwaarden / Benefits
- bonus eligibility
- competitive compensation
- opportunity for impact on patient outcomes
- career development and leadership
- regular collaboration with senior leaders
- meaningful work in health tech
Verantwoordelijkheden
- Lead the clinical evidence strategy across the product lifecycle to enable regulatory approvals, claims, and lifecycle management.
- Collaborate with Product Management, R&D, Regulatory, Quality, Medical Affairs, HE&MA, Marketing, and senior leadership to align evidence plans with portfolio strategy.
- Drive global clinical studies and real-world evidence programs; oversee scientific publications and clinical communications.
- Represent Philips externally with regulators, notified bodies, investigators, and scientific partners.
- Build, develop, and retain a high-performing Clinical Affairs team with clear goals and career development.
Belangrijkste vereisten
- 10+ years of progressive experience in Clinical Affairs, clinical development, or evidence generation in medical devices, digital health, or related healthcare tech.
- 5+ years of people-leadership experience in a global, matrixed organization.
- Strong track record developing and executing clinical evidence strategies that support regulatory approval, market access, and adoption.
- Solid understanding of clinical research methodology and global regulatory requirements (GCP, ISO 14155, FDA/EU medical device regulations).
- cross-functional collaboration
- influencing and stakeholders management
- strategic thinking
- clinical evidence generation
- regulatory compliance (GCP, ISO 14155, FDA/EU)
- real-world evidence programs
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