Research Associate

Há 4 dias


Lisboa, Lisboa, Portugal ICON Tempo inteiro

The Role of a Clinical Research Associate is critical in the conduct of clinical trials. At ICON, we are committed to providing our CRAs with the tools, resources, and support necessary to excel in their roles.

This position involves coordinating the setup and monitoring of studies, preparing and submitting regulatory documents, and reviewing and analyzing study data.

We are seeking a highly skilled and motivated individual to join our team as a Senior CRA/CRA II. Key qualifications include:

  • At least 18 months of experience in clinical research monitoring, preferably with a CRO or pharmaceutical company
  • Strong understanding of ICH-GCP guidelines and ability to apply them effectively
  • Excellent written and verbal communication skills, with proficiency in both Portuguese and English
  • Proven ability to work accurately under pressure and meet deadlines
  • A valid driver's license and willingness to travel within Portugal

We offer a competitive salary package, comprehensive health insurance, and opportunities for professional growth and development.



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