Studienkoordinator:in / Clinical Research Coordinator / Study Nurse (m/w/d)

IQVIA

Trier, Germany
Coordination and patient care
Data management and documentation
Patient recruitment and screening
You will take on a central role in the daily study routine and work closely with the investigator team

Job Summary

  • You will take on a central role in the daily study routine and work closely with the investigator team.
  • The role involves coordination and support of a clinical study under delegation of the Principal Investigator.
  • You will be responsible for ensuring patient well-being and professional patient and visit management.

Matching Summary

You will take on a central role in the daily study routine and work closely with the investigator team.

Skills & Requirements

Must-have

  • Coordination and patient care
  • Data management and documentation
  • Patient recruitment and screening
  • Collaboration with monitors
  • Structured and patient-oriented work

Nice-to-have

  • Experience with blood draws
  • Experience with EKGs

Key Requirements

  • Minimum 2 years clinical research experience
  • Proficient in EDC systems
  • Excellent German language skills
  • Good IT skills (MS Office)

Work Rights

Not specified

Tailored Resume

Cover Letter