Netherlands, Eindhoven
Fulltime: 40 uur per week
Ervaring: N.v.t.
Opleiding: Phd. / Doctoraat
Medische apparatuur
Uiterlijke sollicitatiedatum: 08 juni 2025

Solliciteren

Introductie

Ready to make a real impact? As a Clinical Development Scientist, you ensure that Philips' innovative medical products are safe and effective. Your work contributes directly to global product approvals and improved patient outcomes. You'll collaborate with cross-functional experts and regulatory bodies while working on meaningful projects that truly matter.

Functieomschrijving

You'll be involved throughout the clinical development lifecycle:

  • Conduct benefit-risk assessments and support risk management throughout the product lifecycle.
  • Collect, appraise, and analyze clinical data to support product safety and performance.
  • Write and maintain high-quality documentation such as Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-up (PMCF) reports.
  • Collaborate with internal stakeholders (regulatory affairs, statisticians, risk management, etc.) and external parties (consultants, authorities) to deliver strong clinical evidence.
  • Support clinical investigations and product submissions in the US, EU, and other global markets.
  • Lead clinical risk assessments from early development through to market launch.
  • Review and optimize procedures and workflows within the Clinical Development team.

Vereisten

You have strong analytical skills, a structured mindset, and a passion for innovation in healthcare. You communicate effectively and enjoy working in multidisciplinary teams. In addition, you have:

  • A Master's, M.D., or Ph.D. in Biomedical Sciences, Medicine, or a related field.
  • 3-5 years of experience in the medical device or pharmaceutical industry.
  • Expertise in benefit-risk analysis and clinical risk management.
  • Experience in clinical writing, systematic reviews, and data appraisal; familiarity with MDR-compliant CERs and PMCFs is a plus.
  • Solid knowledge of GCP, ICH guidelines, ISO14155, FDA, and EU regulations.
  • A good understanding of clinical study design, biostatistics, and research methodology.
  • Professional fluency in English, both written and spoken.

Arbeidsvoorwaarden

  • Monthly salary between €4500 and €5500.
  • 26 vacation days with the option to buy more.
  • Extensive learning and development opportunities through the Brunel Academy.
  • A pension plan and collective health insurance.
  • Discounts on sports, cultural events, and vitality programs.

About Brunel

At Brunel Engineering, we connect exceptional professionals with impactful projects in top-tier organizations. You'll get more than just a contract - we offer coaching, training, and a wide professional network. We invest in your growth, so you can develop your expertise and thrive in a dynamic, results-driven environment.

Contactgegevens vacature

BA

Bo van den Akker

+31 6 23 93 8013