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Medical Research Associate (spitscontract)

ICON
Netherlands
On-site

About this role

About the Role Medical Research Associate at ICON, a peak-time contract role designed to support clinical drug trials during busy periods. You’ll combine caring and research tasks with data handling to help ensure safe, protocol-driven studies and reliable health outcomes for participants.

What You'll Do

  • Perform care- and research-related procedures and collect samples (blood draws, medication dispensation, blood pressure measurements, ECGs) within your training and scope.
  • Collect and register study data in multiple systems.
  • Monitor participants’ health before and after medication administration.
  • Support preparation and execution of clinical studies.
  • Be a point of contact for participants and monitor their wellbeing.
  • Collaborate with physicians, study coordinators, and other disciplines.
  • Maintain your own administration, training, and professional development.

What We're Looking For

  • Minimum MBO-4 level education and thinking level.
  • A completed healthcare-related qualification (e.g., Nursing, Medical Assistant, Medical Assistance, Biomedical Laboratory Technician, HLO or similar).
  • Valid BIG registration is a plus but not required.
  • Experience in healthcare, clinical research, or healthcare-related settings is a plus.
  • Affinity with patient care, clinical research and medical procedures.
  • Accuracy and meticulousness in work.
  • Strong communication skills and an empathetic attitude.
  • Independence and sense of responsibility.
  • Flexibility and availability during peak periods.
  • Willingness to learn and continuously develop.

Nice to Have

  • BIG registration is a plus.
  • Experience with data systems and documentation is advantageous.

Compensation & Benefits

  • Salary according to ICON’s CAO; final scale depends on education and experience.
  • Flexible 0.5 FTE spitscontract, 4 shifts of 5 hours per week; ideal to combine with study, another job or private obligations.
  • Allowances for irregular hours (where applicable).
  • Opportunities to develop via trainings and courses within clinical research.
  • Collaboration with a multidisciplinary team of professionals.
  • A work environment prioritizing quality, safety and personal development.
  • Opportunity to gain experience in clinical drug research and advance your career.
  • Benefits include various annual leave entitlements, health insurance options, retirement planning, LifeWorks 24/7 support, life assurance, and flexible country-specific benefits (e.g., childcare vouchers, bike purchase, gym discounts).

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