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Global Study Coordinator

2 semanas atrás

Lisboa, Lisboa, Portugal Phiture Tempo inteiro

Key Responsibilities

As a Clinical Research Associate at Phiture, you will be responsible for:

  • Submitting protocol, consent documents for ethics/IRB approval, and assisting in preparing regulatory submissions as requested
  • Participating in preparing and reviewing study documentation and feasibility studies for new proposals
  • Balancing sponsor-generated queries efficiently and responsible for study cost-effectiveness

Requirements

To succeed in this role, you will need:

  • 18 months+ of monitoring experience in phase I-III trials as a CRA
  • Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data
  • Excellent written and verbal communication in English

What We Offer

In addition to a competitive salary and benefits package, we offer a dynamic and supportive work environment, where you can make a meaningful contribution to the success of our clients and drive lasting change in the field of clinical research.