Introduction

As a Clinical Study Manager, you play a key role in the successful setup, execution, and optimization of clinical studies within a highly regulated and innovative environment. You ensure studies meet the highest quality and compliance standards while contributing to the development of products that impact people worldwide.

What are you going to do 

  • You coordinate and manage clinical studies in compliance with applicable regulations (such as GCP, ISO, and FDA) and internal procedures.
  • You safeguard study quality and progress through site assessments, on-site and remote monitoring, training, and close-out activities.
  • You support and guide study sites and investigators on protocols, procedures, and regulatory requirements.
  • You analyze study data, track timelines and budgets, and proactively identify risks and improvements to ensure efficiency and data integrity.

Essential skills and knowledge

  • A bachelor's or master's degree in Life Sciences, Biomedical Sciences, or a related field.
  • At least 3-5 years of experience in the medical device, pharmaceutical, or another regulated industry.
  • Experience with clinical research, preferably within medical device studies and knowledge of ISO 14155.
  • Experience with systems such as EDC and CTMS, and strong skills in Microsoft Office.
  • Solid understanding of GCP guidelines and relevant regulations.
  • Experience with documentation, auditing, and data analysis.

What we offer 

  • A gross monthly salary between €4,800 and €5,800 (excluding 8% holiday allowance), depending on experience.
  • 26 vacation days, with the option to extend.
  • Flexible working hours and hybrid working possibilities.
  • Extensive training and career development opportunities, including access to the Brunel Academy.
  • A solid pension scheme and collective health insurance.
  • Access to vitality programs and gym discounts.

About Brunel

Brunel Engineering specializes in connecting highly skilled professionals to challenging projects within technical and life sciences environments.

Brunel offers outstanding individuals a diverse and challenging career within a company that values an open, professional, and collaborative culture. Personal initiative is recognized and rewarded, and you will receive the support, coaching, and training needed for your future career. This is your opportunity to explore a wide range of industries and further develop your expertise in a fast-paced and results-driven environment.

Working via Brunel means stability and growth: you not only receive a contract but also build a strong foundation for a successful career.

Closing: 08 May 2026

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Vacancy reference: TR-283581

SC

Corporate recruiter

Sophie Claessens

+31 6 22216027

Contact