Senior Clinical Development Scientist, CT - Medical Devices

Philips

Best

On-site

EUR 78,000 - 130,000

Full time

14 days+

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Job summary

Philips in the Netherlands is seeking a Senior Clinical Development Scientist, CT to analyze clinical studies and protocols for regulatory compliance, data integrity, and strategic alignment while developing CERs, CSRs, and regulatory submissions. You will generate evidence-based insights and support innovative study designs.

This is an office-based role; for our office-based teams, this means working in-person at least 3 days per week.

Qualifications

5+ years of experience in Clinical Affairs or Clinical Research with proven regulatory-compliant results.
Strong understanding of EU Medical Device Regulations, GCP, and ICH guidelines.
Experience with clinical investigation design, biostatistics, research methodologies, and medical writing.
MSc/PhD/MD/PharmD in Biomedical Sciences or related healthcare field; MDR CER/PMCF experience is a strong plus.
Excellent analytical, communication, and project management skills; fluent in English.

Responsibilities

Collect, appraise and analyze clinical data pertaining to a medical device.
Write CERs and PMCF Reports to support regulatory submission.
Collaborate with internal and external partners to ensure comprehensive analysis of clinical evidence.
Ensure interpretation and dissemination of evidence, including CSRs and CERs, and support timely study publication.
Create procedures and workflows for the Clinical Development department.