Clinical Research Coordinator / Study Nurse (m/w/d) In Teilzeit

IQVIA Inc

Erfurt, Germany
Coordination of clinical research studies
Patient recruitment and screening
Data entry in edc systems
This position involves coordinating clinical research studies while ensuring a safe environment for patients and staff

Job Summary

  • This position involves coordinating clinical research studies while ensuring a safe environment for patients and staff.
  • The role requires managing patient care, data quality, and administrative tasks including CRFs and electronic data capture systems.
  • Candidates must have at least one year of relevant experience or equivalent medical training and education.

Matching Summary

This position involves coordinating clinical research studies while ensuring a safe environment for patients and staff.

Skills & Requirements

Must-have

  • Coordination of clinical research studies
  • Patient recruitment and screening
  • Data entry in EDC systems
  • CRF documentation management
  • Adherence to study protocols

Nice-to-have

  • Strong interpersonal communication skills
  • Experience with MS Office applications
  • Ability to work under Principal Investigator direction
  • Logistical coordination for study procedures

Key Requirements

  • Minimum one year of clinical research experience
  • Medical education or equivalent training
  • Excellent German language skills (written and spoken)
  • Proficiency in MS Windows and Office applications

Work Rights

Not specified

Tailored Resume

Cover Letter