Study Coordinator

TFS HealthScience

Roma, Italy
On-site
Clinical study document management
Patient recruitment and scheduling
Sponsor and ethics committee communication
The Study Coordinator will perform coordination and supervision of clinical studies in various dermatological indications at SCIderm Clinics

Job Summary

  • The Study Coordinator will perform coordination and supervision of clinical studies in various dermatological indications at SCIderm Clinics.
  • Key responsibilities include communication with sponsors, agencies, ethics committees, monitors, and patients, as well as managing study documents and budgets.
  • TFS HealthScience offers opportunities for personal and professional growth in a rewarding environment, valuing collaboration, quality, and making a difference in patients' lives.

Matching Summary

The Study Coordinator will perform coordination and supervision of clinical studies in various dermatological indications at SCIderm Clinics.

Skills & Requirements

Must-have

  • Clinical study document management
  • Patient recruitment and scheduling
  • Sponsor and ethics committee communication
  • ICH-GCP Guidelines and AMG knowledge
  • External service provider coordination

Nice-to-have

  • Quality conscious independent work
  • Collaboration and innovation focus
  • Personal and professional growth opportunities

Key Requirements

  • Minimum 2 years relevant experience
  • Study Nurse/Study Coordinator experience
  • Full university degree in natural science
  • Good regulatory skills
  • Good command of English
  • Good knowledge of MS-Office

Work Rights

Not specified

Tailored Resume

Cover Letter