Clinical Development Scientist

Koninklijke Philips Nederland is een gediversifieerd technologiebedrijf dat het leven van mensen wil verbeteren door zinvolle innovaties op het gebied van gezondheidszorg, consumentenlevensstijl en verlichting. Het bedrijf is marktleider op het gebied van cardiologische zorg, acute zorg en zorg voor thuis, energiezuinige verlichtingsoplossingen en nieuwe verlichtingstoepassingen, en op het gebied van scheerapparaten, haartrimmers en mondverzorgingsproducten.

Are you ready to use your clinical expertise to improve lives around the world? At Philips, you’ll work on life-changing projects that contribute to innovative healthcare solutions, making a lasting impact on global health and well-being.

In this role as a Clinical Development Scientist, you will play a pivotal role in generating, interpreting, and communicating clinical evidence to support high-quality Philips products and solutions. Your work will be essential in ensuring the safety, effectiveness, and regulatory compliance of our medical devices—ultimately improving the lives of billions.

• Collect, appraise, and analyze clinical data related to medical products.
• Contribute to harm reviews based on Risk Management Methodology (RMM), collaborate with physicians, and author medical reports.
• Partner with internal teams such as Regulatory Affairs, Study Management, Biostatistics, Post-Market Surveillance, Risk Management, Legal, and Marketing—as well as with external stakeholders including regulatory authorities, consultants, and subject matter experts.
• Write and review essential clinical documentation: Clinical Study Reports (CSRs), Clinical Evaluation Reports (CERs), and Post-Market Clinical Follow-up (PMCF) Reports. Support the publication of clinical findings.
• Support clinical trial operations and product approvals across global markets, including the US, EU, and Rest of World (RoW).
• Provide clinical risk assessments throughout the product lifecycle—from initial concept to market launch.
• Evaluate safety data from Post-Market Surveillance (PMS), literature reviews, and other sources.
• Integrate safety data into regulatory submissions such as risk-benefit analyses, protocols, CSRs, and CERs.
• Analyze adverse event reports to ensure accurate classification and regulatory compliance.
• Respond to safety-related inquiries from healthcare professionals, patients, and internal teams.
• Assist in developing and implementing safety policies, programs, and procedures.
• Keep abreast of evolving global regulatory requirements to ensure continuous compliance.

Competitive Salary – Aligned with market standards.

13th Month Bonus – Pro-rated and paid periodically.

Holiday Allowance – 8.33% of your annual salary, ensuring you can fully enjoy your time off.

Pension Plus Scheme – Secure your future with our comprehensive retirement plan.

Home Office Setup – Receive a €750 net allowance to create a comfortable and productive workspace.

Time to Recharge – Enjoy 25 vacation days per year (based on a 40-hour workweek).

Travel Allowance – Support for commuting expenses.

Internet Allowance – Contribute to seamless remote work.

Relocation Assistance – Moving to the Netherlands? We’ve got you covered.

Join us and enjoy a rewarding career with outstanding benefits that support your work-life balance!