Clinical Research Associate

Há 7 dias


Oeiras, Lisboa, Portugal IQVIA Argentina Tempo inteiro

In the dynamic environment of IQVIA Argentina, we are seeking a Clinical Research Associate to join our Real World Evidence Department. As a key member of our team, you will support the management of clinical dossiers for clients across various industries.

Job Description

Your primary responsibilities will include:

  • Supporting the health technology assessment (HTA) submission and reimbursement processes, including the preparation of Added Therapeutic Value dossiers and other clinical documentation.
  • Conducting literature reviews and evidence synthesis to support clinical dossiers.
  • Assisting in the preparation and submission of clinical trial applications and other regulatory documents.
  • Collaborating with clinical teams to ensure the accuracy and completeness of clinical data.
  • Contributing to the preparation, execution, and follow-up of client projects.
Key Skills and Qualifications

To be successful in this role, you will need:

  • A degree in life sciences, pharmacy, nursing, or a related field.
  • A postgraduate degree in clinical research, pharmacy, biostatistics, epidemiology, healthcare policy, or another healthcare-related discipline.
  • A strong understanding of clinical research methodologies and of the Portuguese health care system.
  • Previous work experience in clinical or outcomes research, real-world evidence, or evidence generation.
  • Proficiency in Portuguese and English (both written and spoken).
  • Strong communication skills.
  • Excellent execution skills, consistently meeting deadlines.
  • Keenness to learn and commitment to a rapid development curve.
  • A self-driven approach and ability to work in a team.


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