CT Medical Device Clinical Development Scientist

Philips International; Netherlands; Remote; EUR 78,000 - 130,000; Full time

Job summary

Philips, a global health technology company based in the Netherlands, seeks a Senior Clinical Development Scientist, CT, to lead clinical data analysis and regulatory documentation for Computed Tomography products. You will write CERs, PMCFs, CSRs, and support regulatory submissions while aligning evidence with market access strategies.

Requirements include 5+ years in Clinical Affairs or similar, expertise in EU MDR/GCP/ICH, and MSc or higher in a related discipline; English fluency is

Qualifications

• 5+ years of experience in Clinical Affairs or Clinical Research within Medical Device/Healthcare.
• Strong understanding of EU Medical Device Regulations, GCP and ICH guidelines.

Responsibilities

• Collect, appraise and analyze clinical data for medical devices.
• Write CERs, PMCFs and CSRs to support regulatory submissions.
• Collaborate with internal and external partners to ensure comprehensive evidence.
• Create procedures and workflows for Clinical Development.

Skills

Clinical affairs

Regulatory compliance

Data analysis

Scientific writing

Project management

Education

MSc or higher in Biomedical Sciences

Tools

Statistical software

Job description

Philips, a global health technology company based in the Netherlands, seeks a Senior Clinical Development Scientist, CT, to lead clinical data analysis and regulatory documentation for Computed Tomography products. You will write CERs, PMCFs, CSRs, and support regulatory submissions while aligning evidence with market access strategies.

Requirements include 5+ years in Clinical Affairs or similar, expertise in EU MDR/GCP/ICH, and MSc or higher in a related discipline; English fluency is