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

IQVIA UK

Erfurt, Germany
Clinical research study coordination
Patient well-being and quality assurance
Maintaining study documentation
Coordinate clinical research studies and maintain a safe study environment under the direction of the Principal Investigator

Job Summary

  • Coordinate clinical research studies and maintain a safe study environment under the direction of the Principal Investigator.
  • Ensure patient well-being and address their concerns while maintaining the highest quality of care.
  • Support patient enrollment through recruitment, screening, and onboarding according to the study protocol.

Matching Summary

Coordinate clinical research studies and maintain a safe study environment under the direction of the Principal Investigator.

Skills & Requirements

Must-have

  • Clinical research study coordination
  • Patient well-being and quality assurance
  • Maintaining study documentation
  • Logistical planning for study procedures
  • Clinical trial data entry and review
  • Patient recruitment and screening

Nice-to-have

  • Effective working relationships
  • Problem-solving with equipment

Key Requirements

  • Minimum one year relevant clinical research experience
  • Knowledge of clinical study workflows and consent
  • Proficient in MS Windows and Office applications
  • Excellent interpersonal skills
  • Very good German language skills

Work Rights

Not specified

Tailored Resume

Cover Letter