Full-time

Clinical Scientist Risk & Benefit

Posted by Brunel • Eindhoven, North Brabant, Netherlands

📍 Eindhoven, North Brabant 🕒 February 23, 2026

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About the Role

Over deze functie

Lead benefit-risk assessments and clinical risk management activities throughout the full product lifecycle.

Collect, appraise, and analyze clinical data and ensure robust clinical evidence for medical products.

Author and maintain clinical documentation, including Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-up (PMCF) Reports, and Clinical Study Reports (CSRs).

Collaborate with multidisciplinary internal teams (regulatory, risk management, statistics, post-market surveillance) and external stakeholders to ensure compliant and high-quality clinical evidence.

Support clinical investigations, regulatory submissions, and product approvals in the US, EU, and other regions.

Optimize workflows, SOPs, and documentation processes within Clinical Development.

Over jou

A PHD or Master's degree in Life Sciences, Biomedical Sciences, or a related health field...

Job Details

Location Eindhoven, North Brabant
Job Type Full-time
Category Life Scientists
Posted February 23, 2026
Deadline April 04, 2026

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