Introduction

You drive clinical risk management and benefit-risk analysis that directly impact patient safety worldwide. In this role, you translate complex clinical data into clear, compliant evidence that supports innovative medical technologies. You work at the intersection of science, regulation, and product development, influencing decisions from concept to market. If you want real responsibility, regulatory depth, and visible impact, this role delivers.

What are you going to do

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.

Essential skills and knowledge

A PHD or Master's degree in Life Sciences, Biomedical Sciences, or a related health field.
Minimum 2 years of relevant experience in Clinical Research, MedTech, Healthcare, or a related field
Experience with clinical documentation such as CERs, PMCFs, or CSRs is preferred.
Knowledge of GCP, ICH guidelines, ISO 14155, FDA regulations, and EU MDR.
Experience in benefit-risk analysis, clinical risk management, or vigilance reporting is a strong advantage.
Affinity with clinical investigation design, research methodology, and biostatistics.
Professional proficiency in English, both written and spoken.

What we offer

A salary up to € 5.500, - gross per month (excluding 8% holiday allowance).
Travel allowance.
26 holidays, with options to expand.
Flexibility and hybrid working options where applicable.
Extensive training and career development opportunities.
A solid pension scheme and collective health insurance.
Discounts on sports and cultural activities.

About Brunel

Brunel Engineering connects highly skilled specialists to challenging projects within innovative industries such as Life Sciences, High Tech, and Engineering. We offer a professional, open, and performance-driven work culture where initiative is recognized.

Closing: March 26, 2026

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Do you have any questions about this vacancy?

Vacancy reference: TR-279567

GP

Corporate recruiter

Gijs Peters

+31 6 13117389

Contact

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Shape your future

Are you ready for the next step in your career? Join Brunel’s powerful global network, where passionate, results-driven specialists come together with industry-leading clients. By connecting specialists to pioneering projects, we drive change in many industries, enabling growth and delivering great outcomes. Brunel helps you reach your full potential and empowers you to make an impact within a purpose-driven global company.

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Our Culture and Values

At Brunel, we are proud of our unique corporate culture, which is shaped and nurtured by the collective efforts of our employees. Our work environment is characterised by an authentic, communicative and inclusive approach to teamwork that fosters an atmosphere of collaboration and creativity. Our values are at the center of everything we do – for our clients, our colleagues and ourselves.

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Our ESG Commitment

Since 1975, our mission has always been to connect specialists to exciting career opportunities, to support the development of these careers, and to offer fair and equal employment. This has enabled us to create a truly sustainable and durable business model. Having a passion for people and caring deeply for the environment is not only part of Brunel’s DNA but is also reflected in our culture and values. As a global company, we take our social responsibility very seriously.

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