Senior Clinical Development Scientist – IGT

About the role

Philips is seeking a Senior Clinical Development Scientist to lead IGT‑related clinical activities in Shanghai. The role focuses on designing, executing, and reporting clinical studies while ensuring regulatory compliance and strategic alignment.

Key responsibilities

• Analyze clinical trial protocols, ensure regulatory adherence, and recommend protocol optimizations.
• Prepare Clinical Evaluation Reports, Clinical Study Reports, and regulatory submission sections using advanced software tools.
• Troubleshoot data collection and analysis issues to maintain data integrity across studies.
• Synthesize study data for abstracts, white papers, and peer‑reviewed publications.
• Develop clinical development and market access strategies and contribute to protocol development.
• Conduct comprehensive literature reviews to support new product introductions and life‑cycle management.
• Support relationships with key opinion leaders and investigators to facilitate robust study execution.
• Present findings to internal stakeholders and disseminate evidence to external audiences.

Required profile

• Master's degree in Clinical Medicine (MD preferred).
• Minimum 3 years of clinical experience in equipment or device R&D.
• Proven ability to work under supervision while handling complex clinical data.

Required skills

• Regulatory compliance and requirements knowledge.
• Data analysis and interpretation.
• Document auditing.
• Medical writing and report preparation.
• Clinical evaluation methodologies.
• Clinical evidence generation strategy.