CRA 2: On-Site Clinical Trial Monitor Argentina

IQVIA Argentina is hiring a Clinical Research Associate (CRA) to ensure compliance and data integrity in clinical trials. Responsibilities include conducting site visits, training personnel, and monitoring study compliance with regulatory standards.

The ideal candidate has a Bachelor’s degree and at least 1 year of on-site monitoring experience. Strong knowledge of GCP and ICH guidelines is required. This position is crucial for maintaining quality in clinical research across various therapeutic areas including oncology, cardiovascular, and internal medicine.