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Study Support Coordinator

1 settimana fa

Trieste, Friuli Venezia Giulia, Italia IQVIA A tempo pieno

Clinical Research Coordinator Position

We are seeking a highly skilled and organized professional to join our team as a Clinical Research Coordinator.

This role requires 24 hours of work per week for approximately four months.

The successful candidate will be responsible for coordinating study activities, maintaining accurate records, and ensuring compliance with regulations.

Key Tasks:

  • Coordinating study startup, maintenance, and close-out activities;
  • Maintaining accurate and complete study files, including subject information and regulatory documents;
  • Ensuring timely submission of study reports and other documentation;
  • Providing administrative support to the site team, as needed.

The ideal candidate will have excellent communication skills, attention to detail, and the ability to work independently.

Previous experience in clinical research coordination or a related field is preferred.

About Us:

IQVIA is a global leader in the healthcare industry that offers opportunities for professional growth and development.