Clinical Development Scientist

Clinical Development Scientist based in Eindhoven.

• develop and execute clinical evidence strategies to inform product design and performance optimization
• design GCP/ISO 14155‑compliant clinical investigations and oversee early‑development studies
• interpret literature and study data to guide product specifications and future development
• create evidence‑generation plans, literature reviews, clinical study protocols, and Clinical Study Reports (CSRs)
• oversee IRB/IEC submissions, ethics management, and site oversight for clinical studies
• understand mechanisms of action, demonstrate performance and safety, and translate findings into input for future product improvements
• safeguard consumer and product safety through rigorous evidence generation and risk‑based decision making

• MD and/or PhD preferred; MSc in a relevant scientific discipline also invited.
• strong scientific background with experience in clinical evaluation methods.
• 3–5 years of experience in clinical research or clinical development, preferably in medical devices or consumer health.
• experience setting up clinical studies, including ethics submissions and site oversight.
• proven medical/scientific writing skills and ability to critically appraise clinical literature.
• experience collaborating with Biostatistics, Data Management and Regulatory Affairs to ensure robust analysis, data readiness and regulatory compliance.
• excellent communication skills—interpersonal, written, and oral presentation of scientific materials and results.

Office‑based role. Expect in‑person attendance at least 3 days per week.

Philips is an equal opportunity employer. We provide equal employment opportunities to all qualified employees and applicants without regard to race, color, religion, sex, pregnancy, national origin, age, disability, sexual orientation, gender identity or expression, or veteran status. Reasonable accommodations are available for qualified individuals with disabilities.